COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population.

doi:10.1016/j.neurobiolaging.2014.08.006

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Article

COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population.

Neurobiology of aging - 1 Jan 2015

Lin Chin-Hsien, Lin Hang-I, Chen Meng-Ling, Wu Ruey-Meei

Abstract excerpt

A recent collaborative study that combined linkage analysis with whole-genome sequencing of family members of multiplex families with multiple system atrophy (MSA) has identified COQ2 gene as a causative gene for MSA. The common variant, c.T1178C (p.V393A, rs148156462), in the COQ2 gene was found to be associated with an increased risk of sporadic MSA. There is overlapping clinical characteristics between MSA and...

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Source

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Identifiers

PMID: 25200193
DOI: 10.1016/j.neurobiolaging.2014.08.006

Genes

COQ2

Variants

rs148156462

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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