Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?
Identifieur interne : 000C08 ( PubMed/Curation ); précédent : 000C07; suivant : 000C09Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?
Auteurs : S. Lesage [France] ; S. Belarbi ; A. Troiano ; C. Condroyer ; N. Hecham ; P. Pollak ; E. Lohman ; T. Benhassine ; F. Ysmail-Dahlouk ; A. Dürr ; M. Tazir ; A. BriceSource :
- Neurology [ 1526-632X ] ; 2008.
English descriptors
- KwdEn :
- Adolescent, Adult, Africa, Northern, Aged, Aged, 80 and over, Child, Dyskinesias (genetics), Female, Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Male, Middle Aged, Parkinson Disease (genetics), Parkinson Disease (physiopathology), Point Mutation, Protein-Serine-Threonine Kinases (genetics).
- MESH :
- chemical , genetics : Protein-Serine-Threonine Kinases.
- chemical : Leucine-Rich Repeat Serine-Threonine Protein Kinase-2.
- genetics : Dyskinesias, Parkinson Disease.
- physiopathology : Parkinson Disease.
- Adolescent, Adult, Africa, Northern, Aged, Aged, 80 and over, Child, Female, Humans, Male, Middle Aged, Point Mutation.
DOI: 10.1212/01.wnl.0000338460.89796.06
PubMed: 18981379
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