P268S in NOD2 associates with susceptibility to Parkinson’s disease in Chinese population

BACKGROUND: The cause of almost all cases of Parkinson’s disease (PD) remains unknown. Recent years have seen an explosion in the rate of discovery of genetic defects linked to PD. Different racial and geographical populations may have different distributions of genetic variants. METHODS: In the cur...

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Detalhes bibliográficos
Main Authors: Ma, Qilin, An, Xingkai, Li, Zhiming, Zhang, Huanjing, Huang, Wenqing, Cai, Liangliang, Hu, Peng, Lin, Qing, Tzeng, Chi-Meng
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3662627/
https://ncbi.nlm.nih.gov/pubmed/23651603
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-9081-9-19
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