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Article

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

Scientific reports - 3 Oct 2016

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

Abstract excerpt

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) inheritance in the Chinese Han population from mainland China were included in this study. We did not identify any...

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Identifiers

PMID: 27694831
DOI: 10.1038/srep34502
PMCID: PMC5046083

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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