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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...

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Detalhes bibliográficos
Publicado no:Behav Neurol
Main Authors: Zheng, Yifan, Pei, Zhong, Liu, Yanmei, Zhou, Hongyan, Xian, Wenbiao, Fang, Yingying, Chen, Ling, Wu, Qi
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4544948/
https://ncbi.nlm.nih.gov/pubmed/26346174
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/621873
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