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...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2015-01-01
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Series: | Behavioural Neurology |
Online Access: | http://dx.doi.org/10.1155/2015/621873 |