Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.
Identifieur interne : 000092 ( Ncbi/Checkpoint ); précédent : 000091; suivant : 000093Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.
Auteurs : Hao Deng ; Weidong Le ; Yi Guo ; Christine. Hunter ; Wenjie Xie ; Joseph Jankovic [États-Unis]Source :
- Annals of neurology [ 0364-5134 ] ; 2005.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Protein-Serine-Threonine Kinases.
- geographic : North America.
- genetics : Parkinson Disease.
- Aged, Female, Humans, Male, Middle Aged, Point Mutation.
DOI: 10.1002/ana.20510
PubMed: 15929036
Affiliations:
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pubmed:15929036Le document en format XML
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