Mutation analysis of PARK2 in a Uyghur family with early-onset Parkinson's disease in Xinjiang, China
β Scribed by Li, Hongyan; Yusufujiang, Aishanjiang; Naser, Shaliya; Zhu, Yi; Maimaiti, Mayinur; He, Xiaoyan; Bu, Juan; Meng, Xuegang; Wang, Mingyuan; Li, Jiang; Dina, Baiting; Yang, Lijuan; Nayi, Zuhere; Dang, Hui; Wang, Chengfeng; Amiti, Dilimulati; Aji, Asiya; Yusufu, Nazuke; Jiao, Yan; Duan, Fengmei
- Book ID
- 123142502
- Publisher
- Elsevier Science
- Year
- 2014
- Tongue
- English
- Weight
- 499 KB
- Volume
- 342
- Category
- Article
- ISSN
- 0022-510X
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## Abstract Mutations in __LRRK2__ (__leucineβrich repeat kinase 2__) have been associated with autosomal dominant Parkinson's disease (PD) and cluster in several 3β² exons of the gene. The majority of mutations have been detected in lateβonset cases (age at onset >50 years). We screened 5 of the 51