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Article

Association analysis of polymorphisms in VMAT2 and TMEM106B genes for Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy.

Journal of the neurological sciences - 15 Jun 2017

Hu Tao, Chen Yongping, Ou Ruwei, Wei Qianqian, Cao Bei, Zhao Bi, Wu Ying, Song Wei, Chen Xueping, Shang Hui-Fang

Abstract excerpt

BACKGROUND: The vesicular monoamine transporter type 2 (VMAT2) and transmembrane Protein 106B (TMEM106B) were reported to be associated with neurodegenerative diseases. Recent studies found that two polymorphisms (rs363371 and rs363324) in VMAT2 might be a risk factor for Parkinson's disease (PD) in Caucasians, while the two other variants (rs1990622 and rs3173615) in TMEM106B increased the risk for...

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Identifiers

PMID: 28477711
DOI: 10.1016/j.jns.2017.03.028

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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