𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutation analysis of PARK2 in a Uyghur family with early-onset Parkinson's disease in Xinjiang, China

✍ 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

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Recurrent LRRK2 (Park8) mutations in ear
✍ Katja Hedrich; Susen Winkler; Johann Hagenah; Kemal Kabakci; Meike Kasten; Eberh πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 95 KB πŸ‘ 1 views

## Abstract Mutations in __LRRK2__ (__leucine‐rich repeat kinase 2__) have been associated with autosomal dominant Parkinson's disease (PD) and cluster in several 3β€² exons of the gene. The majority of mutations have been detected in late‐onset cases (age at onset >50 years). We screened 5 of the 51