Identification of VPS35 mutations replicated in French families with Parkinson disease.
Identifieur interne : 000802 ( PubMed/Checkpoint ); précédent : 000801; suivant : 000803Identification of VPS35 mutations replicated in French families with Parkinson disease.
Auteurs : S. Lesage [France] ; C. Condroyer ; S. Klebe ; A. Honoré ; F. Tison ; C. Brefel-Courbon ; A. Dürr ; A. BriceSource :
- Neurology [ 1526-632X ] ; 2012.
Descripteurs français
- Wicri :
- geographic : France.
English descriptors
- KwdEn :
- Adult, Aged, Alleles, DNA Mutational Analysis, Female, France, Genetic Testing, Genetic Variation (genetics), Genetics, Population, Haplotypes, Heterozygote Detection, Humans, Male, Middle Aged, Mutation, Missense (genetics), Parkinson Disease (diagnosis), Parkinson Disease (genetics), Polymorphism, Single Nucleotide (genetics), Vesicular Transport Proteins (genetics).
- MESH :
- chemical , genetics : Vesicular Transport Proteins.
- geographic : France.
- diagnosis : Parkinson Disease.
- genetics : Genetic Variation, Mutation, Missense, Parkinson Disease, Polymorphism, Single Nucleotide.
- Adult, Aged, Alleles, DNA Mutational Analysis, Female, Genetic Testing, Genetics, Population, Haplotypes, Heterozygote Detection, Humans, Male, Middle Aged.
DOI: 10.1212/WNL.0b013e318253d5f2
PubMed: 22517097
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
pubmed:22517097Le document en format XML
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