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Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China

✍ Scribed by Qing-Zhou Fei; Li Cao; Qin Xiao; Ting Zhang; Lan Zheng; Xi-Jin Wang; Gang Wang; Hai-Yan Zhou; Ying Wang; Sheng-Di Chen


Book ID
116772143
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
128 KB
Volume
475
Category
Article
ISSN
0304-3940

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## 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