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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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| Publicado no: | Behav Neurol |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2015
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| 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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