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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)...

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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

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