Genetic analysis of indel markers in three loci associated with Parkinson's disease

The causal mutations and genetic polymorphisms associated with susceptibility to Parkinson’s disease (PD) have been extensively described. To explore the potential contribution of insertion (I)/deletion (D) polymorphisms (indels) to the risk of PD in a Chinese population, we performed genetic analys...

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Detalles Bibliográficos
Autores principales: Huo, Zhixin, Luo, Xiaoguang, Zhan, Xiaoni, Chu, Qiaohong, Xu, Qin, Yao, Jun, Pang, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584932/
https://www.ncbi.nlm.nih.gov/pubmed/28873462
http://dx.doi.org/10.1371/journal.pone.0184269

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584932/
https://www.ncbi.nlm.nih.gov/pubmed/28873462
http://dx.doi.org/10.1371/journal.pone.0184269

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