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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Detalles Bibliográficos
Autores principales: Zheng, Yifan, Pei, Zhong, Liu, Yanmei, Zhou, Hongyan, Xian, Wenbiao, Fang, Yingying, Chen, Ling, Wu, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544948/
https://www.ncbi.nlm.nih.gov/pubmed/26346174
http://dx.doi.org/10.1155/2015/621873

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544948/
https://www.ncbi.nlm.nih.gov/pubmed/26346174
http://dx.doi.org/10.1155/2015/621873

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