RAB39B gene mutations are not linked to familial Parkinson’s disease in China

Recently, RAB39B mutations were reported to be a causative factor in patients with Parkinson’s disease (PD). To validate the role of RAB39B in familial PD, a total of 195 subjects consisting of 108 PD families with autosomal-dominant (AD) inheritance and 87 PD families with autosomal-recessive (AR)...

Descripción completa

Detalles Bibliográficos
Autores principales: Kang, Ji-feng, Luo, Yang, Tang, Bei-sha, Wan, Chang-min, Yang, Yang, Li, Kai, Liu, Zhen-hua, Sun, Qi-ying, Xu, Qian, Yan, Xin-xiang, Guo, Ji-feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046083/
https://www.ncbi.nlm.nih.gov/pubmed/27694831
http://dx.doi.org/10.1038/srep34502

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046083/
https://www.ncbi.nlm.nih.gov/pubmed/27694831
http://dx.doi.org/10.1038/srep34502

Ejemplares similares