Cognitive Impairments inLRRK2-Related Parkinson’s Disease: A Study in Chinese Individuals
Abstract
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 aimed to explore the effects of LRRK2 S1647T polymorphism on cognitive function in PD. Method . 90 PD patients were randomly recruited. They underwent...
Paper Details
Title
Cognitive Impairments inLRRK2-Related Parkinson’s Disease: A Study in Chinese Individuals
Published Date
Jan 1, 2015
Journal
Volume
2015
Pages
1 - 5
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