Cognitive Impairments in LRRK2-Related Parkinson’s Disease: A Study in Chinese Individuals

Background. LRRK2 S1647T has been identified as a polymorphic risk variant for Parkinson’s disease (PD) in Chinese individuals. As LRRK2 is the most common genetic cause for PD, it has drawn great interest regarding whether cognitive impairments in PD are related with LRRK2. Purpose. This study ai...

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Bibliographic Details
Main Authors: Yifan Zheng, Zhong Pei, Yanmei Liu, Hongyan Zhou, Wenbiao Xian, Yingying Fang, Ling Chen, Qi Wu
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:Behavioural Neurology
Online Access:http://dx.doi.org/10.1155/2015/621873

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