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Caption : Accreditation =Accreditation ;

    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Movement Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of Dystonia-parkinsonism, Paisan-Ruiz type (PLA2G6 gene: sequencing / MLPA)
    • Centogene AG
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of Dystonia-parkinsonism, Paisan-Ruiz type (PLA2G6 gene: sequencing)
    • CeGaT GmbH
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of Hallervorden-Spatz disease (PANK2 gene)
    • Istituto CSS-Mendel
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of dystonia-parkinsonism, Paisan-Ruiz type (PLA2G6 gene)
    • Sistemas Genómicos S.L.
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of neurodegeneration with brain iron accumulation (PLA2G6 gene: targeted mutation analysis and deletion/duplication analysis by MLPA)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Molecular diagnosis of Parkinson disease (ATP13A2, C19ORF12, PARK7, PINK1, PLA2G6 genes)
    • Technische Universität München
    • More information
    • ITALY
    • CALABRIA
    • MANGONE
    • Molecular diagnosis of Hallervorden-Spatz disease (CP, FTL, PANK2, PLA2G6 genes)
    • CNR
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of dystonia-parkinsonism, Paisan-Ruiz type (PLA2G6 gene)
    • CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
    • More information
    • POLAND
    • Lodz
    • LODZ
    • Molecular diagnosis of Hallervorden-Spatz syndrome (PANK2 gene)
    • Uniwersytecki Szpital Kliniczny
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
    • Medizinische Universität Wien
    • More information