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LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China

✍ Scribed by Lihua Yu; Fayun Hu; Xiaoyi Zou; Yi Jiang; Yan Liu; Xianghua He; Jing Xi; Ling Liu; Zhuolin Liu; Li He; Yanming Xu


Book ID
113504509
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
141 KB
Volume
1296
Category
Article
ISSN
0006-8993

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LRRK2 R1628P variant is a risk factor of
✍ Zijuan Zhang; Jean-Marc Burgunder; Xingkai An; Yan Wu; Wenjun Chen; Jinhong Zhan πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 66 KB

## 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