Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's disease.
Identifieur interne : 004716 ( Main/Merge ); précédent : 004715; suivant : 004717Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's disease.
Auteurs : G. Lucotte ; G. Mercier ; J C TurpinSource :
- Journal of neurology, neurosurgery, and psychiatry [ 0022-3050 ] ; 1998.
Descripteurs français
- Wicri :
- geographic : France.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Nerve Tissue Proteins, Phosphoproteins.
- geographic : France, Synucleins, alpha-Synuclein.
- genetics : Parkinson Disease, Point Mutation.
- Adult, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Periodicity.
PubMed: 9854985
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pubmed:9854985Le document en format XML
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