## Abstract Mutations in __LRRK2__, the gene that encodes leucine‐rich repeat kinase 2 (LRRK2), are associated with autosomal dominant and sporadic forms of Parkinson's disease (PD) and are the most common genetic causes of PD. Recently, a R1628P variant has been reported as a risk factor for PD in
✦ LIBER ✦
LRRK2 Gly2385Arg variant is a risk factor of Parkinson’s disease among Han-Chinese from mainland China
✍ Scribed by X.-K. An; R. Peng; T. Li; J.-M. Burgunder; Y. Wu; W.-J. Chen; J.-H. Zhang; Y.-C. Wang; Y.-M. Xu; Y.-R. Gou; G.-G. Yuan; Z.-J. Zhang
- Book ID
- 111065397
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 96 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1351-5101
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