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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Detalles Bibliográficos
Autores principales: Ma, Qilin, An, Xingkai, Li, Zhiming, Zhang, Huanjing, Huang, Wenqing, Cai, Liangliang, Hu, Peng, Lin, Qing, Tzeng, Chi-Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662627/
https://www.ncbi.nlm.nih.gov/pubmed/23651603
http://dx.doi.org/10.1186/1744-9081-9-19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662627/
https://www.ncbi.nlm.nih.gov/pubmed/23651603
http://dx.doi.org/10.1186/1744-9081-9-19

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