Novel and de novo mutations of the SGCE gene in Brazilian patients with myoclonus‐dystonia
Identifieur interne : 002D11 ( Main/Exploration ); précédent : 002D10; suivant : 002D12Novel and de novo mutations of the SGCE gene in Brazilian patients with myoclonus‐dystonia
Auteurs : Vanderci Borges [Brésil] ; Patricia De Carvalho Aguiar [Brésil] ; Henrique Ballalai Ferraz [Brésil] ; Laurie J. Ozelius [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-06-15.
Descripteurs français
- Wicri :
- geographic : Brésil.
English descriptors
- KwdEn :
- Adult, Brazil, DNA Mutational Analysis, Disease Progression, Dystonia (complications), Dystonia (ethnology), Dystonia (genetics), Gene Expression, Genotype, Humans, Male, Microsatellite Repeats, Mutation (genetics), Myoclonus (complications), Myoclonus (ethnology), Myoclonus (genetics), Sarcoglycans (genetics).
- MESH :
- chemical , genetics : Sarcoglycans.
- geographic : Brazil.
- complications : Dystonia, Myoclonus.
- ethnology : Dystonia, Myoclonus.
- genetics : Dystonia, Mutation, Myoclonus.
- Adult, DNA Mutational Analysis, Disease Progression, Gene Expression, Genotype, Humans, Male, Microsatellite Repeats.
Url:
DOI: 10.1002/mds.21380
Affiliations:
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Le document en format XML
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