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: Accreditation
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- GERMANY
- Nordrhein-Westfalen
- BOCHUM
- Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2, PLA2G6 genes)
- Ruhr-Universität Bochum
- More information
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- GERMANY
- Rheinland-Pfalz
- INGELHEIM AM RHEIN
- Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2, PLA2G6 genes: sequencing, MLPA)
- Bioscientia Institut für Medizinische Diagnostik GmbH
- More information
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Unexplained Movement Disorders (exome sequencing)
- Radboudumc - Radboud universitair medisch centrum
- More information
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
- Radboudumc - Radboud universitair medisch centrum
- More information
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- GERMANY
- Mecklenburg-Vorpommern
- ROSTOCK
- Molecular diagnosis of neurodegeneration with brain iron accumulation (FA2H- PANK2, PLA2G6 genes)
- Centogene AG
- More information
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- GERMANY
- Mecklenburg-Vorpommern
- ROSTOCK
- Molecular diagnosis of Dystonia-parkinsonism, Paisan-Ruiz type (PLA2G6 gene: sequencing / MLPA)
- Centogene AG
- More information
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of neurodegeneration with brain iron accumulation (C19ORF12, PLA2G6, PANK2, FTL genes: sequencing)
- CeGaT GmbH
- More information
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of Dystonia-parkinsonism, Paisan-Ruiz type (PLA2G6 gene: sequencing)
- CeGaT GmbH
- More information
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- Molecular diagnosis of Hallervorden-Spatz disease (PANK2 gene)
- Istituto CSS-Mendel
- More information
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- SPAIN
- Comunidad Valenciana
- PATERNA
- Molecular diagnosis of dystonia-parkinsonism, Paisan-Ruiz type (PLA2G6 gene)
- Sistemas Genómicos S.L.
- More information
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- 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
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- Molecular diagnosis of neurodegeneration with brain iron accumulation (ATP13A2, C19ORF12, FA2H, FTL, PANK2, PLA2G6 genes)
- Technische Universität München
- More information
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- Molecular diagnosis of Parkinson disease (ATP13A2, C19ORF12, PARK7, PINK1, PLA2G6 genes)
- Technische Universität München
- More information
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- Molecular diagnosis of neurodegeneration with brain iron accumulation (PANK2, PLA2G6 genes: sequencing, MLPA)
- Gemeinschaftspraxis für Humangenetik
- More information
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- Molecular diagnosis of Hallervorden-Spatz disease (CP, FTL, PANK2, PLA2G6 genes)
- CNR
- More information
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- 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
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- Molecular diagnosis of Hallervorden-Spatz syndrome (PANK2 gene)
- Uniwersytecki Szpital Kliniczny
- More information
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- Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
- Medizinische Universität Wien
- More information
