Caption
: Accreditation
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Unexplained Movement Disorders (exome sequencing)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- More information
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- SWITZERLAND
- Suisse Alémanique
- AARGAU
- Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene sequencing and deletion analysis)
- Kantonsspital Aargau
- More information
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene)
- CeGaT GmbH
- More information
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- NETHERLANDS
- Utrecht
- UTRECHT
- Biochemical screening for Hemolytic Anemia due to Red Cell Membrane Disorder (Pre-incubated osmotic fragility test)
- UMC Utrecht - Universitair Medisch Centrum Utrecht
- More information
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- SPAIN
- Galicia
- SANTIAGO DE COMPOSTELA
- Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene)
- CHUS - Complejo Hospitalario Universitario de Santiago
- More information
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- SPAIN
- Baleares
- PALMA DE MALLORCA
- Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene)
- Hospital Universitario Son Espases
- More information
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- Molecular diagnosis of McLeod neuroacanthocytosis syndrome (XK gene)
- CNR
- More information
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- Molecular diagnosis of neuroacanthocytosis (XK, JPH3, VPS13A genes)
- Fundació Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol
- More information
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- Molecular diagnosis of McLeod neuroacanthocytosis syndrome (aCGH)
- Genetadi Biotech S.L.
- More information