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Caption : Accreditation =Accreditation ;

    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA1, SCA2, SCA3, SCA6, SCA7, SCA17, ATXN8, ATXN10, PPP2R2B and DRPLA genes)
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Molecular diagnosis of Huntington-like 1 disease (PRNP gene)
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Molecular diagnosis of Huntington-like 2 disease (JPH3 gene)
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENČVE
    • Accreditation
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 17 genes)
    • Centre Médical Universitaire - CMU
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENČVE
    • Accreditation
    • Molecular diagnosis of dentatorubral - Pallidoluysian Atrophy (ATN1 gene)
    • Centre Médical Universitaire - CMU
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Ruhr-Universität Bochum
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1-3, 6, 7, 17 (ATXN1-3, CACNA1A, ATXN7, TBP genes)
    • Ruhr-Universität Bochum
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2, PLA2G6 genes)
    • Ruhr-Universität Bochum
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Accreditation
    • Molecular diagnosis of Neuroferritinopathy (FTL gene)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7 (ATXN1-3, ATXN7, CACNA1A genes)
    • Labor Lademannbogen
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Labor Lademannbogen
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of Huntington disease (HTT and JPH3 genes)
    • Universitätsklinikum Ulm
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Universitätsklinikum Ulm
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1-3, 6-8, 12, 14, 17 (ATXN1-3, CACNA1A, ATXN7, ATXN8, PPP2R2B, PRKCG, TBP genes)
    • Universitätsklinikum Ulm
    • More information
    • SPAIN
    • Cataluńa
    • BARCELONA
    • Accreditation
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia. Genes ATXN1 / SCA1, ATXN2 / SCA2, ATXN3 / SCA3, CACNA1A / SCA6, ATXN7 / SCA7, ATXN8 / SCA8 genes
    • Laboratorio de Análisis Dr. Echevarne
    • More information
    • SPAIN
    • Cataluńa
    • BARCELONA
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy
    • Laboratorio de Análisis Dr. Echevarne
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7, 8, 17 (ATXN1, ATXN2, ATXN3, ATXN7, ATXN8, CACNA1A, TBP genes)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of choreoacanthocytosis (VPS13A gene)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Schleswig-Holstein
    • LÜBECK
    • Accreditation
    • Molecular diagnosis of Huntington disease, HDL2 and HDL4 (HTT, JPH3 and TBP genes)
    • Universitätsklinikum Schleswig-Holstein - Campus Lübeck
    • More information
    • GERMANY
    • Schleswig-Holstein
    • LÜBECK
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Universitätsklinikum Schleswig-Holstein - Campus Lübeck
    • More information
    • GERMANY
    • Schleswig-Holstein
    • LÜBECK
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1-3, 6-8, 10-14, 17, 27, 28 (AFG3L2, ATXN1-3, ATXN7, ATXN10, CACNA1A, C10orf2, FGF14, KCNC3, PPP2R2B, PRKCG, TBP, TTBK2 genes)
    • Universitätsklinikum Schleswig-Holstein - Campus Lübeck
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Molecular diagnosis of dentatorubral-pallidoluysian Atrophy (ATN1 gene)
    • Genetica AG
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Molecular diagnosis of Huntington disease-like 2 (JPH3 gene)
    • Genetica AG
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 8, 10, 12, 17 genes)
    • Genetica AG
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Molecular diagnosis of pantothenate kinase-associated neurodegeneration (PANK2 gene)
    • Genetica AG
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1-3, 6, 7, 17 (ATXN1-3, CACNA1A(CAG repeat), ATXN7, TBP genes)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2, PLA2G6 genes: sequencing, MLPA)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene: repeats)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Molecular diagnosis of SCA1: Spinocerebellar ataxia type 1 (ATX1 gene)
    • University Hospitals Leuven - Gasthuisberg
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Molecular diagnosis of SCA2: Spinocerebellar ataxia type 2 (ATX2 gene)
    • University Hospitals Leuven - Gasthuisberg
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Molecular diagnosis of SCA3: Spinocerebellar ataxia type 3 (ATX3 gene)
    • University Hospitals Leuven - Gasthuisberg
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Accreditation
    • Molecular diagnosis of Dentatorubral pallidoluysian atrophy (DRPLA gene)
    • CHU de LIEGE - UniLab Lg
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of Dentatorubral - Pallidolysian Atrophy (DRPLA gene)
    • Centre Hospitalier Universitaire Vaudois - CHUV
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of autosomal dominant Spinocerebellar Ataxia (SCA1, 2, 3, 6, and 7)(ATXN1, ATXN2, ATXN3, CACNA1A and ATXN7 genes)
    • Centre Hospitalier Universitaire Vaudois - CHUV
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular diagnosis of Dentatorubral pallidoluysian atrophy (DRPLA gene)
    • University and University Hospital of Antwerp - UZA
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA1,2,3,6,7,8,10,12,17) (ATX1, ATX2, ATX3, CACNA1A, ATX7, PPP2R2B, TPB genes)
    • University and University Hospital of Antwerp - UZA
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular diagnosis of SCA1: Spinocerebellar ataxia type 1 (ATX1 gene)
    • University and University Hospital of Antwerp - UZA
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular diagnosis of SCA2: Spinocerebellar ataxia type 2 (ATX2 gene)
    • University and University Hospital of Antwerp - UZA
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular diagnosis of SCA3: Spinocerebellar ataxia type 3 (ATX3 gene)
    • University and University Hospital of Antwerp - UZA
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular diagnosis of SCA17: Spinocerebellar ataxia type 17 (TPB gene)
    • University and University Hospital of Antwerp - UZA
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (DRPLA gene)
    • Erasme Hospital - ULB
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Accreditation
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA1,2,3,6,7) (ATX1, ATX2, ATX3, CACNA1A, ATX7 genes)
    • Erasme Hospital - ULB
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Dentatorubral Pallidoluysian Atrophy (DRPLA)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Pantothenate Kinase Associated Neurodegeneration (PANK2 gene)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 1 (ATXN1 gene)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Neuroferritinopathy - Neurodegeneration with brain iron accumulation (FTL gene)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 2 (ATXN2 gene)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 3 (ATXN3 gene)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Spinocerebellar ataxia type 17 -SCA17 (TBP gene)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Dentatorubral Pallidoluysian Atrophy - DRPLA (ATN1 gene: analysis of CAG trinucleotide repeat by PCR)
    • Sheffield Children's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 1 (ATXN1 gene)
    • Sheffield Children's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 2 (ATXN2 gene)
    • Sheffield Children's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 3 (ATXN3 gene)
    • Sheffield Children's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Strathclyde
    • GLASGOW
    • Accreditation
    • Molecular diagnosis of Dentatorubral Pallidoluysian Atrophy (DRPLA)
    • Southern General Hospital
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of Autosomal Dominant Cerebellar Ataxia type 1 (ADCAI) - SCA1, SCA2 and SCA3 (ATXN1, ATXN2 and ATXN3 genes)
    • Birmingham Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of Dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • Birmingham Women's NHS Foundation Trust
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6
    • Medizinische Genetik Dresden
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 1 (ATXN1 gene)
    • University Hospital of Wales NHS Trust
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 2 (ATXN2 gene)
    • University Hospital of Wales NHS Trust
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 3 (ATXN3 gene)
    • University Hospital of Wales NHS Trust
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 17 (TBP gene)
    • University Hospital of Wales NHS Trust
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2 gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Dentatorubral pallidoluysian atrophy (DRPLA gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of SCA1: Spinocerebellar ataxia type 1(ATXN1 gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of SCA2: Spinocerebellar ataxia type 2 (ATXN2 gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of SCA17: Spinocerebellar ataxia type 17 (TPB gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of SCA3: Spinocerebellar ataxia type 3 (ATXN3 gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Pantothenate Kinase-Associated Neurodegeneration / Hallervorden-Spatz syndrome (PANK2 gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Spinocerebellar ataxia type 1 (ATXN1 gene)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 3 (ATXN3 gene)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 2 (ATXN2 gene)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 17 (TBP gene)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of benign familial Chorea (TITF1 gene)
    • VUmc - VU medisch centrum
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • ROTTERDAM
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Erasmus MC, Faculteitsgebouw
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • ROTTERDAM
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 1 (ATXN1 gene)
    • Erasmus MC, Faculteitsgebouw
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • ROTTERDAM
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 2 (ATXN2 gene)
    • Erasmus MC, Faculteitsgebouw
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • ROTTERDAM
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 3 (ATXN3 gene)
    • Erasmus MC, Faculteitsgebouw
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • LEIDEN
    • Accreditation
    • Molecular diagnosis of Dentatorubral-Pallydoluysian Atrophy (ATN1 gene)
    • LUMC - Leids Universitair Medisch Centrum
    • More information
    • NETHERLANDS
    • Groningen
    • GRONINGEN
    • Accreditation
    • Molecular diagnosis of Autosomal Dominant Cerebellar Ataxia (ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A and PDYN gene)
    • UMCG - Universitair Medisch Centrum Groningen
    • More information
    • NETHERLANDS
    • Groningen
    • GRONINGEN
    • Accreditation
    • Molecular diagnosis of Pantothenate Kinase-Associated Neurodegeneration (PANK2 gene)
    • UMCG - Universitair Medisch Centrum Groningen
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 1 (ATXN1 gene)
    • Addenbrooke's Hospital
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Molecular diagnosis of Dentatorubral Pallidoluysian Atrophy (DRPLA gene)
    • Addenbrooke's Hospital
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 2 (ATXN2 gene)
    • Addenbrooke's Hospital
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 3 (ATXN3 gene)
    • Addenbrooke's Hospital
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 17 (TBP gene)
    • Addenbrooke's Hospital
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Autosomal Dominant Spinocerebellar Ataxia (ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A, PP2R2B, PRKCG, TBP, KCNC3, PDYN and AFG3L2 gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Dentatorubral Pallidoluysian Atrophy (DRPLA gene)
    • International Centre for Life
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Neuroferritinopathy (Neurodegeneration with brain iron accumulation)
    • International Centre for Life
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 1 (ATXN1 gene)
    • International Centre for Life
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 2 (ATXN2 gene)
    • International Centre for Life
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 3 (ATXN3 gene)
    • International Centre for Life
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 17 (TBP gene)
    • International Centre for Life
    • More information
    • UNITED KINGDOM
    • County Antrim
    • BELFAST
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 1 (ATXN1 gene)
    • Belfast City Hospital
    • More information
    • UNITED KINGDOM
    • County Antrim
    • BELFAST
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 2 (ATXN2 gene)
    • Belfast City Hospital
    • More information
    • UNITED KINGDOM
    • County Antrim
    • BELFAST
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 3 (ATXN3 gene)
    • Belfast City Hospital
    • More information
    • UNITED KINGDOM
    • County Antrim
    • BELFAST
    • Accreditation
    • Molecular diagnosis of Spinocerebellar Ataxia type 17 (TBP gene)
    • Belfast City Hospital
    • More information
    • GERMANY
    • Thüringen
    • JENA
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7 (ATXN1-3, CACNA1A genes)
    • Universitätsklinikum Jena
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7 (ATXN1-3, ATXN7, CACNA1A genes)
    • Zentrum für Humangenetik und Laboratoriumsmedizin Dr. Klein und Dr. Rost
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1-8, 10-18, 27, 31 (ATXN1-3, ATXN7, ATXN8OS, ATXN10, CACNA1A, FGF14, IFRD1, ITPR1, KCNC3, PLEKHG4, PPP2R2B, PRKCG, SPTBN2, SYNE1, TBP, TTBK2 genes)
    • Institute of Molecular Diagnostics
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of Huntington disease, HDL1 and HDL2 (HTT, JPH3 and PRNP genes)
    • Institute of Molecular Diagnostics
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Institute of Molecular Diagnostics
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of Huntington disease-like 1 and 2 (PRNP, JPH3 genes)
    • Institute of Molecular Diagnostics
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (FA2H- PANK2, PLA2G6 genes)
    • Institute of Molecular Diagnostics
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of choreoacanthocytosis (VPS13A gene)
    • Institute of Molecular Diagnostics
    • More information
    • GERMANY
    • Baden-Württemberg
    • KARLSRUHE
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6 (ATXN1-3, CACNA1A genes)
    • Labor Prof. Seelig & Kollegen
    • More information
    • SWEDEN
    • Skane
    • LUND
    • Accreditation
    • Molecular diagnosis of Dentatorubral Pallidoluysian Atrophy (ATN1 gene: fragment analysis)
    • University Hospital
    • More information
    • SWEDEN
    • Skane
    • LUND
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene: fragment analysis)
    • University Hospital
    • More information
    • SWEDEN
    • Skane
    • LUND
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene: fragment analysis)
    • University Hospital
    • More information
    • SWEDEN
    • Skane
    • LUND
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene: fragment analysis)
    • University Hospital
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of spinocerebellar ataxia type 1-7, 10-14, 17, 27 (ATXN1-3, ATXN7, ATXN8, ATXN10, C10orf2, CACNA1A, FGF14, KCNC3, PLEKHG4, PPP2R2B, PRKCG, SPTBN2, TBP genes)
    • MVZ Fenner & Krasemann
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of Huntington disease, HDL1 and HDL2 (HTT, JPH3 and PRNP genes)
    • MVZ Fenner & Krasemann
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • AARGAU
    • Accreditation
    • Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene sequencing and deletion analysis)
    • Kantonsspital Aargau
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PLA2G6, PANK2 and FTL genes: sequencing)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of choreoacanthocytosis (VPS13A gene: sequencing)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of familial benign chorea (NKX2-1 gene)
    • CeGaT GmbH
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Molecular diagnosis of Huntington and Huntington-like diseases (HTT, JPH3 genes)
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of neuroferritinopathy (FTL gene)
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of pantothenate kinase associated neurodegeneration (PANK2 gene)
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of brain-lung-thyroid syndrome and benign familial chorea (NKX2-1 gene)
    • CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of spinocerebellar ataxia type1, 2, 3, 6, 7 and 17 (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7 and TBP genes)
    • CHRU de Lille - Centre de biologie et pathologie
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • CHRU de Lille - Centre de biologie et pathologie
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of Huntington disease-like 2 (JPH3 gene)
    • CHRU de Lille - Centre de biologie et pathologie
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of benign familial chorea (NKX2-1 gene)
    • CHRU de Lille - Centre de biologie et pathologie
    • More information
    • FRANCE
    • POITOU-CHARENTES
    • POITIERS
    • Molecular diagnosis of spinocerebellar ataxia type 1
    • CHU de Poitiers
    • More information
    • FRANCE
    • POITOU-CHARENTES
    • POITIERS
    • Molecular diagnosis of spinocerebellar ataxia type 2
    • CHU de Poitiers
    • More information
    • FRANCE
    • POITOU-CHARENTES
    • POITIERS
    • Molecular diagnosis of spinocerebellar ataxia type 3
    • CHU de Poitiers
    • More information
    • FRANCE
    • ALSACE
    • SCHILTIGHEIM
    • Preimplantation genetic diagnosis of autosomal dominant spinocerebellar ataxia (SCA2 and SCA3 genes)
    • Centre Médico-Chirurgical et Obstétrical (CMCO)
    • More information
    • FRANCE
    • ALSACE
    • SCHILTIGHEIM
    • Preimplantation genetic diagnosis of spinocerebellar ataxia type 17 (TBP gene)
    • Centre Médico-Chirurgical et Obstétrical (CMCO)
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • CHU d'Angers
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia, type 1 (ATXN1 gene)
    • CHU d'Angers
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia, type 2 (ATXN2 gene)
    • CHU d'Angers
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia, type 3 (ATXN3 gene)
    • CHU d'Angers
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia, type 17 (TBP gene)
    • CHU d'Angers
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of Huntington disease-like 2 (JPH3 gene)
    • CHU d'Angers
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of dentatorubral pallidolusyan atrophy (DRPLA gene)
    • Azienda Ospedaliero-Universitaria San Giovanni Battista di Torino
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 8, 10, 12, 17)
    • Azienda Ospedaliero-Universitaria San Giovanni Battista di Torino
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of neuroferritinopathy (FTL gene)
    • Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of benign familial chorea (NKX2-1 gene)
    • Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2, PLA2G6 genes)
    • Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of cerebellar ataxia, type 1, 2, 3, 5, 6, 7, 8, 10, 12, 13, 14, 17, 27,36 (ATXN1, ATXN2, ATXN3, SPTBN2, CACNA1A, ATXN7, ATXN8OS, ATXN10, PPP2R2B, PRKCG, TBP, FGF14, NOP56 genes)
    • B.I.R.D. Foundation
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of Huntington disease-like 2 (JPH3 gene)
    • B.I.R.D. Foundation
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of Huntington disease-like 1(PRNP gene)
    • B.I.R.D. Foundation
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of familial benign chorea (NKX2-1, sequencing)
    • B.I.R.D. Foundation
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • B.I.R.D. Foundation
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of autosomal dominant dominant cerebellar ataxia (SCA 1, 2, 3, 6, 7, 8, 10, 12, 17) (ATXN1, ATXN2, ATXN3, ATXN7, ATXN8, ATXN10, TBP, CACNA1A, PPP2R2B genes)
    • Azienda Ospedaliera Universitaria Policlinico di Tor Vergata
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Azienda Ospedaliera Universitaria Policlinico di Tor Vergata
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of benign familial chorea (NKX2-1 gene)
    • Azienda Ospedaliera Universitaria Policlinico di Tor Vergata
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of Huntington disease, type 1 and type 2 (IT15, PRNP, JPH3 genes)
    • CNR - Dipartimento di Medicina
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 12, 14, 17, 27) (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, PPP2R2B, PRKCG, TBP, FGF14 genes)
    • CNR - Dipartimento di Medicina
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of familial benign chorea (NKX2-1 gene)
    • CNR - Dipartimento di Medicina
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • CNR - Dipartimento di Medicina
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 17 (ATXN1, ATXN2, ATXN3, CACNA1A, TBP genes)
    • Biotecnologie Avanzate Srl
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 17)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of dentatorubral pallidolysian atrophy (ATN1 gene)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7, 8, 10, 12 and 17 (ATXN1-3, ATXN10, ATXN7, ATXN8OS, CACNA1A, PPP2R2B, TBP, genes)
    • Praxis für medizinische Genetik
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • AACHEN
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7, 8 and 17 (ATXN1-3, ATXN7, ATXN8OS, CACNA1A, TBP genes)
    • Universitätsklinikum Aachen
    • More information
    • SPAIN
    • Asturias
    • OVIEDO
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (detection of expanded alleles in ATN1 gene)
    • Hospital Universitario Central de Asturias
    • More information
    • SPAIN
    • Asturias
    • OVIEDO
    • Molecular diagnosis of autosomal dominant cerebellar ataxia (detection of expanded alleles in ATXN1, PPP2R2B, TBP, ATXN2, ATXN3, CACNA1A, ATXN7 and ATXN8 genes)
    • Hospital Universitario Central de Asturias
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7) (ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A genes)
    • Laboratorio Genoma
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of pantothenate-kinase associated neurodegeneration (PANK2 gene)
    • Laboratorio Genoma
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Universitätsklinikum Freiburg
    • More information
    • GERMANY
    • Hessen
    • GIEßEN
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen
    • More information
    • GERMANY
    • Hessen
    • GIEßEN
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7 , 17 and 23 (ATXN1-3, ATXN7, CACNA1A, PDYN, PRKCG, TBP genes)
    • Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7 and 17 (ATXN1-3, ATXN7, CACNA1A, TBP genes)
    • Universitätsmedizin Göttingen
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Universitätsmedizin Göttingen
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA1,2,3,6,7,8)
    • Centro de Análisis Genéticos
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy
    • Centro de Análisis Genéticos
    • More information
    • GERMANY
    • Bayern
    • BAD STEBEN
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6
    • Institut für angewandte Humangenetik und Onkogenetik
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of autosomal dominant cerebellar ataxia (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, PPP2R2B, TBP genes)
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of pantothenate kinase-associated neurodegeneration (PANK2 gene)
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene)
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6)
    • IRCCS Ospedale San Raffaele
    • More information
    • SPAIN
    • Cataluńa
    • L'HOSPITALET DE LLOBREGAT
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene)
    • IDIBELL - Instituto de Investigación Biomédica de Bellvitge
    • More information
    • SPAIN
    • Cataluńa
    • L'HOSPITALET DE LLOBREGAT
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene)
    • IDIBELL - Instituto de Investigación Biomédica de Bellvitge
    • More information
    • SPAIN
    • Cataluńa
    • L'HOSPITALET DE LLOBREGAT
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene)
    • IDIBELL - Instituto de Investigación Biomédica de Bellvitge
    • More information
    • SPAIN
    • Cataluńa
    • L'HOSPITALET DE LLOBREGAT
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene)
    • IDIBELL - Instituto de Investigación Biomédica de Bellvitge
    • More information
    • SPAIN
    • Cataluńa
    • L'HOSPITALET DE LLOBREGAT
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • IDIBELL - Instituto de Investigación Biomédica de Bellvitge
    • More information
    • SPAIN
    • Cataluńa
    • L'HOSPITALET DE LLOBREGAT
    • Molecular diagnosis of Huntington disease-like 2. JPH3 gene
    • IDIBELL - Instituto de Investigación Biomédica de Bellvitge
    • More information
    • GERMANY
    • Bayern
    • REGENSBURG
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7 (ATXN1-3, ATXN7, CACNA1A genes)
    • Gemeinschaftspraxis Dr. Susanne Ebner und Dr. Susanne Markus
    • More information
    • GERMANY
    • Bayern
    • REGENSBURG
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Gemeinschaftspraxis Dr. Susanne Ebner und Dr. Susanne Markus
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Molecular diagnosis of spinocerebellar ataxia type 1-3, 6-8, 10-14, 17, 27 (ATXN1-3, ATXN7, ATXN8OS, ATXN10, CACNA1A, FGF14, KCNC3, PPP2R2B, PRKCG, TBP, TTBK2 genes)
    • Universitätsklinikum Tübingen
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Universitätsklinikum Tübingen
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Molecular diagnosis of familial benign chorea (NKX2-1 gene)
    • Universitätsklinikum Tübingen
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • FERRARA
    • Molecular diagnosis of spinocerebellar ataxia (SCA 1, 2, 3, 6, 7) (ATX1, ATX2, ATX3, ATX6, ATX7 genes)
    • Azienda Ospedaliero-Universitaria di Ferrara
    • More information
    • SPAIN
    • Baleares
    • PALMA DE MALLORCA
    • Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene)
    • Hospital Universitario Son Espases
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular diagnosis of autosomal dominant cerebellar ataxias (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, ATXN8, ATXN10, PPP2R2B, ATN1 and TBP genes)
    • Hospital Universitario Virgen del Rocío
    • More information
    • FINLAND
    • Finland
    • TURKU
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene)
    • University of Turku
    • More information
    • FINLAND
    • Finland
    • TURKU
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene)
    • University of Turku
    • More information
    • FINLAND
    • Finland
    • TURKU
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene)
    • University of Turku
    • More information
    • FINLAND
    • Finland
    • TURKU
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene)
    • University of Turku
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia type 1 (ATXN1 gene)
    • CHU Paris-GH La Pitié Salpętričre-Charles Foix - Hôpital Pitié-Salpętričre
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of Huntington disease-like 2 (JPH3 gene)
    • CHU Paris-GH La Pitié Salpętričre-Charles Foix - Hôpital Pitié-Salpętričre
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia type 2 (ATXN2 gene)
    • CHU Paris-GH La Pitié Salpętričre-Charles Foix - Hôpital Pitié-Salpętričre
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia type 3 (ATXN3 gene)
    • CHU Paris-GH La Pitié Salpętričre-Charles Foix - Hôpital Pitié-Salpętričre
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia type 17 (TBP gene)
    • CHU Paris-GH La Pitié Salpętričre-Charles Foix - Hôpital Pitié-Salpętričre
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • CHU Paris-GH La Pitié Salpętričre-Charles Foix - Hôpital Pitié-Salpętričre
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Huntington (HD) and Huntinton-like diseases (HDL1, HDl2, HDL4) (HD, PRNP, JPH3 and TBP genes): target mutation analysis - CAG expansion for all genes and fragments analysis for HTT e PRNP genes
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of autossomal dominant spinocerebellar ataxia type 1, 2, 3, 6, 7, 10, 14, 17 and DRPLA (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, ATXN10, TTBK2, PPP2R2B, PRKCG, TBP, KCNC3, IFRD1, FGF14, SPTBN2, ATN1 genes)
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of neuroacanthocytosis (VSP13A gene): sequencing of entire coding region
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of neuroferritinopathy (FTL gene): Sequencing of entire coding region
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of benign familial chorea disease (NKX2-1 gene) by sequencing of entire coding region
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of pantothenate-kinase-associated neurodegeneration, NBIA1, e.g. Hallervorden-spatz syndrome (PANK2 gene): sequencing of entire coding region and delection/duplication analysis by MLPA
    • Instituto de Biologia Molecular e Celular
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of neuroferritinopathy disease, NBIA3, (FTL gene): sequencing of the entire coding region
    • Instituto de Biologia Molecular e Celular
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene)
    • Hospital Universitario La Fe (Campanar)
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Molecular diagnosis of Huntington disease-like 2 (JPH3 gene)
    • Hospital Universitario La Fe (Campanar)
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Molecular diagnosis of Huntington disease-like 1 (PRNP gene)
    • Hospital Universitario La Fe (Campanar)
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • Sistemas Genómicos S.L.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of neuroferritinopathy (FTL gene)
    • Sistemas Genómicos S.L.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene)
    • Sistemas Genómicos S.L.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene)
    • Sistemas Genómicos S.L.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene)
    • Sistemas Genómicos S.L.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of pantothenate-kinase-associated neurodegeneration (PANK2 gene)
    • Sistemas Genómicos S.L.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene)
    • Sistemas Genómicos S.L.
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHWERZENBACH
    • Molecular diagnosis of Dentatorubral-pallidolysian atrophy (DRPLA gene): triplet repeat expansion
    • Universität Zürich
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHWERZENBACH
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7 and 8): CAG expansion
    • Universität Zürich
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia types 1, 2, 3 and 6 (SCA1, SCA2, SCA3 and CACNA1A genes)
    • Tartu University Hospital
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2 gene)
    • Praxis Dres. Gencik
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6 and 17 (ATXN1-3, CACNA1A, TBP genes)
    • Praxis Dres. Gencik
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of Neuroferritinopathy (FTL gene)
    • Praxis Dres. Gencik
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7, and 17 (ATXN1, 2, 3, and 7, CACNA1A, and TBP genes)
    • Medizinische Universität Wien
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • Medizinische Universität Wien
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of pantothenate kinase-associated neurodegeneration (PANK2 gene)
    • Medizinische Universität Wien
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular diagnosis of choreoacanthocytosis (VPS13A gene): sequencing of the entire coding region.
    • Faculdade de Medicina da Universidade de Lisboa
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia: SCA 1, 2, 3, 6, 7, 8, 12 and 17 (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, ATXN8, PP2R2B, TBP genes)
    • Fundación Jiménez Díaz
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • Fundación Jiménez Díaz
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of spinocerebellar ataxia (C10ORF2, ATXN1, 2, 3, 7, 8, and 10, CACNA1A, TTBK2, PPP2R2B, KCNC3, PRKCG, TBP, TDP1, and SETX genes)
    • Praxis für Humangenetik
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of pantothenate kinase-associated neurodegeneration (PANK2 gene)
    • Praxis für Humangenetik
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Neuroferritinopathy (FTL gene)
    • Praxis für Humangenetik
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Huntington disease-like 1 (PRNP gene)
    • Praxis für Humangenetik
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • Praxis für Humangenetik
    • More information
    • SPAIN
    • Cataluńa
    • BARCELONA
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • Hospital Clínic de Barcelona
    • More information
    • SPAIN
    • Cataluńa
    • BARCELONA
    • Molecular diagnosis of autosomal dominant cerebellar ataxia (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, ATXN8 and ATN1 genes)
    • Hospital Clínic de Barcelona
    • More information
    • HUNGARY
    • Dél-Dunántúl
    • PECS
    • Molecular diagnosis of spinocerebellar ataxia type 1,2,3,6,7 and 17 (ATXN1, ATXN2, ATXN3, CACNA1A , ATXN7 and TBP genes)
    • Clinical Center - University of Pécs
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Molecular diagnosis of spinocerebellar ataxia types 1,2,3,6,7,8,12 and 17 (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, SCA8, PPP2R2B, TBP genes)
    • The Cyprus Institute of Neurology and Genetics
    • More information
    • CYPRUS
    • Cyprus
    • NICOSIA
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (DRPLA gene)
    • The Cyprus Institute of Neurology and Genetics
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene): CAG repeat expansion mutation analysis by TP-PCR
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Cataluńa
    • BARCELONA
    • Preimplantation genetic diagnosis of the spinocerebellar ataxia type 2. ATXN2/SCA2 gene
    • Reprogenetics Spain S.A.
    • More information
    • SPAIN
    • Cataluńa
    • BARCELONA
    • Preimplantation genetic diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene)
    • Reprogenetics Spain S.A.
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of SCA3 or MJD: Spinocerebellar ataxia type 3 (ATX3 gene, trinucleotide repeats)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of Dentatorubral pallidoluysian atrophy (ATN1 gene, trinucleotide repeats)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of SCA1: Spinocerebellar ataxia type 1 (ATX1 gene, trinucleotide repeats)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of SCA17: Spinocerebellar ataxia type 17 (TPB gene, trinucleotide repeats)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of SCA2: Spinocerebellar ataxia type 2 (ATX2 gene, trinucleotide repeats)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (ATP13A2, C19ORF12, FA2H, FTL, PANK2, PLA2G6 genes)
    • Technische Universität München
    • More information
    • NORWAY
    • Řstlandet
    • OSLO
    • Molecular diagnosis of Hallervorden-Spatz disease (PANK2 gene)
    • Oslo University Hospital, Ullevaal
    • More information
    • NORWAY
    • Řstlandet
    • OSLO
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (DRPLA gene)
    • Oslo University Hospital, Ullevaal
    • More information
    • NORWAY
    • Řstlandet
    • OSLO
    • Molecular diagnosis of spinocerebellar ataxia, type 1, 2, 3, 6, 7
    • Oslo University Hospital, Ullevaal
    • More information
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Molecular diagnosis of Spinocerebellar Ataxia type 1 (ATXN1 gene)
    • Western General Hospital
    • More information
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Molecular diagnosis of Spinocerebellar Ataxia type 2 (ATXN2 gene)
    • Western General Hospital
    • More information
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Molecular diagnosis of Spinocerebellar Ataxia type 3 (ATXN3 gene)
    • Western General Hospital
    • More information
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Molecular diagnosis of Dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • Western General Hospital
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2 gene)
    • Motol university hospital - 2nd Medical School Charles University Prague
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Postnatal molecular diagnosis of spinocerebellar ataxias type 1, 2, 6 and 7 (ATXN1, ATXN2, CACNA1A and ATXN7 genes)
    • Motol university hospital - 2nd Medical School Charles University Prague
    • More information
    • NORWAY
    • Vestlandet
    • BERGEN
    • Molecular diagnosis of spinocerebellar ataxia 1, 2, 3, 6 and 7 (ATXN1, ATXN2, ATXN3, CACNA1A and ATXN7 genes)
    • Haukeland University Hospital
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of spinocerebellar ataxia types 1, 2, 3, 6, 7, 8, 10 and 12
    • Acibadem healthcare group
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (DRPLA gene)
    • Acibadem healthcare group
    • More information
    • SPAIN
    • País Vasco
    • BARAKALDO
    • Molecular Diagnosis of Chorea familial benign. Sequentiation of the gene TTF1 / KKX2.2.
    • Hospital Universitario Cruces - Osakidetza
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Karolinska University Hospital - Solna
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA1,2,3,6,7)
    • Karolinska University Hospital - Solna
    • More information
    • CROATIA
    • CROATIA
    • ZAGREB
    • Molecular diagnosis of Spinocerebellar Ataxia type 1
    • Zagreb Clinical Hospital Center
    • More information
    • CROATIA
    • CROATIA
    • ZAGREB
    • Molecular diagnosis of Spinocerebellar Ataxia type 2
    • Zagreb Clinical Hospital Center
    • More information
    • CROATIA
    • CROATIA
    • ZAGREB
    • Molecular diagnosis of Spinocerebellar Ataxia type 3
    • Zagreb Clinical Hospital Center
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Molecular diagnosis of Spino Cerebellar Ataxia (SCA1, SCA2, SCA3, SCA6, SCA7 , Mutation analysis, PGD)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Molecular diagnosis of Spino Cerebellar Ataxia (DRPLA , Mutation analysis)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • More information
    • AUSTRIA
    • TIROL
    • INNSBRUCK
    • Molecular diagnosis of spinocerebellar ataxia (SCA-1, SCA-2, SCA-3, SCA-6, DRPLA)
    • Medizinische Universität Innsbruck
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene: CAG repeat identification)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene: CAG repeat identification)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene: CAG repeat identification)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of Huntington disease, HDL1 and HDL2 (HTT, JPH3 and PRNP genes)
    • Diagenom GmbH
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2 gene)
    • Diagenom GmbH
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of spinocerebellar ataxia type 1-8, 10, 12-14, 17 and 27 (ATXN1-3, ATXN7, ATXN8OS, ATXN10, CACNA1A, FGF14, KCNC3, PLEKHG4, PPP2R2B, PRKCG, SPTBN2 and TBP genes)
    • Diagenom GmbH
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene: CAG repeat identification)
    • Instytut Psychiatrii i Neurologii - Institute of Psychiatry and Neurology
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene: CAG repeat identification)
    • Instytut Psychiatrii i Neurologii - Institute of Psychiatry and Neurology
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene: CAG repeat identification)
    • Instytut Psychiatrii i Neurologii - Institute of Psychiatry and Neurology
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene: CAG repeat identification)
    • Instytut Psychiatrii i Neurologii - Institute of Psychiatry and Neurology
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene: CAG repeat identification)
    • Instytut Psychiatrii i Neurologii - Institute of Psychiatry and Neurology
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Pränatalzentrum Hamburg und Humangenetik
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7 (ATXN1-3, ATXN7, CACNA1A genes)
    • Pränatalzentrum Hamburg und Humangenetik
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy. PCR amplification for the expansion of CAG trinucleotide in ATN1 gene
    • GENETAQ
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of benign familial chorea (NKX2-1 gene)
    • GENETAQ
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of spinocerebellar ataxia (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, ATXN8OS, ATXN10, TBP genes) (Panel SCA1, SCA2, SCA3, SCA6, SCA7) (Panel SCA1, SCA2, SCA3, SCA6, SCA7, SCA8, SCA10, SCA17)
    • GENETAQ
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of pantothenate-kinase-associated neurodegeneration (PANK2 gene - entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of benign familial chorea (NKX2-1 gene - entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of choreoacanthocytosis (VPS13A gene - entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2 gene: sequencing, MLPA)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of Huntington disease, HDL1 and HDL2 (HTT, JPH3 and PRNP genes: sequencing)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene: sequencing)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • GERMANY
    • Sachsen
    • LEIPZIG
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6 and 17 (ATXN1-3, CACNA1A, TBP genes)
    • Universitätsklinikum Leipzig AöR
    • More information
    • SPAIN
    • La Rioja
    • LOGROŃO
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • More information
    • SPAIN
    • La Rioja
    • LOGROŃO
    • Molecular diagnosis of pantothenate-kinase-associated neurodegeneration (PANK2 gene)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • More information
    • SPAIN
    • La Rioja
    • LOGROŃO
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • More information
    • SPAIN
    • La Rioja
    • LOGROŃO
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • More information
    • SPAIN
    • La Rioja
    • LOGROŃO
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • More information
    • SPAIN
    • Cataluńa
    • TERRASSA
    • Molecular diagnostic of autosomal dominant cerebellar ataxia (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, ATXN8, ATN1 genes)
    • Consorci Sanitari de Terrassa
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 15/16, 17, 28)
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of spinocerebellar ataxia (SCA 1, 2, 3, 6, 7,12, 17)
    • Azienda Ospedaliera Universitaria "Federico II"
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy
    • Azienda Ospedaliera Universitaria "Federico II"
    • More information
    • ITALY
    • SICILIA
    • TROINA
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 8)
    • IRCCS OASI Maria Santissima
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA1, 2, 3, 6, 7, 8, 12, 17) (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, ATXN8, PPP2R2B, TBP genes)
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy
    • Azienda Ospedaliera Universitaria Careggi
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 8, 12, 17)
    • Azienda Ospedaliera Universitaria Careggi
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene)
    • IRCCS Azienda Ospedaliera Universitaria S. Martino
    • More information
    • ITALY
    • MOLISE
    • POZZILLI
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 8, 10, 12, 14, 17)
    • Istituto Neurologico Mediterraneo - IRCCS Neuromed
    • More information
    • ITALY
    • MOLISE
    • POZZILLI
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy
    • Istituto Neurologico Mediterraneo - IRCCS Neuromed
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 12, 17) (ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A, PPP2R2B, TBP genes)
    • Policlinico Universitario "A. Gemelli"
    • More information
    • ITALY
    • TOSCANA
    • SIENA
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 8, 12, 17) (SCA8, PPP2R2B, TBP genes)
    • Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
    • More information
    • ITALY
    • LOMBARDIA
    • BRESCIA
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7, 17 (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, TBP genes)
    • Universitŕ degli Studi di Brescia
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Universitätsklinikum Rostock
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of spinocerebellar ataxia type 1-8, 10, 12, 13, 14, 17, 27 (ATXN1-3, ATXN7, ATXN10, C10orf2, CACNA1A, FGF14, KCNC3, PLEKHG4, PPP2R2B, PRKCG, SPTBN2, TBP genes)
    • Universitätsklinikum Rostock
    • More information
    • ITALY
    • CALABRIA
    • MANGONE
    • Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene)
    • CNR
    • More information
    • ITALY
    • CALABRIA
    • MANGONE
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, 8, 12, 14, 17)
    • CNR
    • More information
    • ITALY
    • CALABRIA
    • MANGONE
    • Molecular diagnosis of pantothenate-kinase-associated neurodegeneration (PANK2 gene)
    • CNR
    • More information
    • ITALY
    • CALABRIA
    • MANGONE
    • Molecular diagnosis of neuroferrinopathies (FTL and FTH genes)
    • CNR
    • More information
    • ITALY
    • SICILIA
    • TROINA
    • Molecular diagnosis of spinocerebellar ataxia SCA1, 2, 3, 6, 7, 8 (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7, ATXN8, ATXN8OS genes)
    • IRCCS OASI Maria Santissima
    • More information
    • ITALY
    • TOSCANA
    • SIENA
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1, 2, 3, 6, 7, Machado-Joseph disease) (ATXN1, ATXN2, ATXN3 and CACNA1A genes)
    • Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
    • More information
    • PORTUGAL
    • NORTE
    • BRAGA
    • Molecular diagnosis of Neuroferritinopathy (FTL gene)
    • Instituto de Cięncias da Vida e da Saúde - Universidade do Minho
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA1,2,3,6,7,8,10,12)
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Bichemical diagnosis of chorea-acanthocytosis (chorein expression westernblot from erythrocyte membranes)
    • Ludwig-Maximilians-Universität München
    • More information
    • ITALY
    • LOMBARDIA
    • BOSISIO PARINI
    • Molecular diagnosis of autosomal dominant spinocerebellar ataxia (SCA 1,2)
    • IRCCS "E. Medea"
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of Cerebellar ataxia, autosomal dominant . ATXN1,2,3,7,8, CACNA1A, PPP2R2B and TBP genes.
    • Universidad Complutense de Madrid. Facultad de Medicina
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Clinical diagnosis and epidemiology of spongiforme encephalopathy
    • Universitätsmedizin Göttingen
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6 (ATXN1-3, CACNA1A genes)
    • LMU Klinikum der Universität München - Campus Großhadern
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular diagnosis of autosomal dominant cerebellar ataxias type 1,2,3,6,7. ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7 genes
    • Área Hospitalaria Hospital Universitario Virgen de la Macarena
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy. ATN1 gene
    • Área Hospitalaria Hospital Universitario Virgen de la Macarena
    • More information
    • ITALY
    • LOMBARDIA
    • MONZA
    • Molecular diagnosis of neuroferritinopathy (FTL gene)
    • Consorzio per la Genetica Molecolare Umana
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Molecular diagnosis of familial benign chorea (NKX2-1 gene)
    • Universitätsklinikum Ulm
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene)
    • Medgene s.r.o.
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene)
    • Medgene s.r.o.
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene)
    • Medgene s.r.o.
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene)
    • Medgene s.r.o.
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of dentatorubral pallidoluysian atrophy (ATN1 gene)
    • Medgene s.r.o.
    • More information
    • POLAND
    • Kraków
    • CRACOW
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene)
    • CM UJ Jagiellonian University Medical College
    • More information
    • POLAND
    • Kraków
    • CRACOW
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene)
    • CM UJ Jagiellonian University Medical College
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Molecular diagnosis of familial benign chorea (NKX2-1 gene)
    • Hertie-Institut für klinische Hirnforschung
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Molecular diagnosis of Huntington disease (HTT and JPH3 genes)
    • Hertie-Institut für klinische Hirnforschung
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Molecular diagnosis of spinocerebellar ataxia type 1, 2, 3, 6, 7 and 17 (ATXN1-3, ATXN7, CACNA1A, TBP genes)
    • Hertie-Institut für klinische Hirnforschung
    • More information
    • SPAIN
    • Cataluńa
    • BADALONA
    • Molecular diagnosis of neuroacanthocytosis (XK, JPH3, VPS13A genes)
    • Fundació Institut d'Investigació en Cičncies de la Salut Germans Trias i Pujol
    • More information
    • SPAIN
    • Cataluńa
    • BADALONA
    • Molecular diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene)
    • Fundació Institut d'Investigació en Cičncies de la Salut Germans Trias i Pujol
    • More information
    • SPAIN
    • Cataluńa
    • BADALONA
    • Molecular diagnosis of spinocerebellar ataxia type 2 (ATXN2 gene)
    • Fundació Institut d'Investigació en Cičncies de la Salut Germans Trias i Pujol
    • More information
    • SPAIN
    • Cataluńa
    • BADALONA
    • Molecular diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene)
    • Fundació Institut d'Investigació en Cičncies de la Salut Germans Trias i Pujol
    • More information
    • SPAIN
    • Cataluńa
    • BADALONA
    • Molecular diagnosis of spinocerebellar ataxia type 17 (TBP gene)
    • Fundació Institut d'Investigació en Cičncies de la Salut Germans Trias i Pujol
    • More information
    • SPAIN
    • Cataluńa
    • BADALONA
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • Fundació Institut d'Investigació en Cičncies de la Salut Germans Trias i Pujol
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of autosomal dominant cerebellar ataxia type 1 (entire coding sequence of KCNC3 and FGF14 genes; analysis of CAG triplet expansion in ATXN1, ATXN2, ATXN3 and PPP2R2B genes; analysis of (CTA)(CTG) expansion in ATXN8 gene; analysis of CAA/CAG expansion in TBP gene)
    • LABORATORIO DE GENÉTICA CLÍNICA S.L.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (analysis of CAG triplet expansion in DRPLA gene)
    • LABORATORIO DE GENÉTICA CLÍNICA S.L.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of benign familial chorea (entire coding sequence of NKX2-1 gene)
    • LABORATORIO DE GENÉTICA CLÍNICA S.L.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of Huntington disease-like 2 (analysis of CTG triplet expansion in JPH3 gene)
    • LABORATORIO DE GENÉTICA CLÍNICA S.L.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of pantothenate-kinase-associated neurodegeneration (entire coding sequence of PANK2 gene / deletions-duplications by MLPA analysis)
    • LABORATORIO DE GENÉTICA CLÍNICA S.L.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of choreoacanthocytosis (entire coding sequence of VPS13A gene)
    • LABORATORIO DE GENÉTICA CLÍNICA S.L.
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Molecular diagnosis of spinocerebellar ataxia types 1, 2, 3, 6, 7 and 8 (ATXN1, ATXN2, ATXN3, CACNA1A, ATXN7 and ATXN8 genes)
    • INNOVAGENOMICS, S.L
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (ATN1 gene)
    • INNOVAGENOMICS, S.L
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of neuroferritinopathy (entire coding sequence of FTL gene)
    • LORGEN G.P.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of dentatorubral-pallidoluysian atrophy (ATN1 gene / analysis of CAG triplet expansion)
    • LORGEN G.P.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of spinocerebellar ataxia type 1 (entire coding sequence of SCA1 gene)
    • LORGEN G.P.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of spinocerebellar ataxia type 17 (entire coding sequence of TBP gene)
    • LORGEN G.P.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of spinocerebellar ataxia type 2 (entire coding sequence of ATXN2 gene)
    • LORGEN G.P.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of spinocerebellar ataxia type 3 (entire coding sequence of ATXN3 gene)
    • LORGEN G.P.
    • More information
    • SPAIN
    • País Vasco
    • DERIO
    • Molecular diagnosis of McLeod neuroacanthocytosis syndrome (aCGH)
    • Genetadi Biotech S.L.
    • More information
    • DENMARK
    • Jylland
    • AARHUS
    • Molecular diagnosis of spinocerebellar ataxia (type 1, 2, 3, 6, 7)
    • Aarhus University Hospital - Skejby
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Preimplantation genetic diagnosis of spinocerebellar ataxia type 1 (ATXN1 gene)
    • Iviomics SL
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Preimplantation genetic diagnosis of spinocerebellar ataxia type 3 (ATXN3 gene)
    • Iviomics SL
    • More information
    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Molecular diagnosis of neuroferritinopathy (FTL gene / sequencing)
    • GenoClinics
    • More information