Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literature.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Mar 2016

Zhao QuanZhen, Yang Xinglong, Tian SiJia, An Ran, Zheng JinHua, Xu Yanming

Abstract excerpt

Recent studies in Japan have associated multiple system atrophy (MSA), a neurodegenerative disease of uncertain etiology, with polymorphism in the COQ2 gene. This led us to explore whether the same polymorphism is associated with MSA in Han Chinese and more broadly in East Asians. We conducted a case-control study with 82 Han Chinese with probable MSA and 484 gender- and age-matched healthy subjects, genotyping...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alkyl and Aryl Transferases
Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Multiple System Atrophy

Share to Taiwan

Source

Identifiers

PMID: 26590992
DOI: 10.1007/s10072-015-2414-8

Genes

COQ2

Variants

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literature.PMID 26590992Read ↗

Association of the COQ2 V393A Variant with Parkinson's Disease: A Case-Control Study and Meta-Analysis.Semantic proximity Read ↗

Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy.Semantic proximity Read ↗

Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy.Semantic proximity Read ↗

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

COQ2 variants in Parkinson's disease and multiple system atrophy.Semantic proximity Read ↗

Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese population.Semantic proximity Read ↗

[Susceptibility gene in multiple system atrophy (MSA)].Semantic proximity Read ↗

Cross-examining candidate genes implicated in multiple system atrophySemantic proximity Read ↗

Genome-wide association study identifies a new susceptibility locus in <i>PLA2G4C</i> for Multiple System AtrophySemantic proximity Read ↗

Plasma Coenzyme Q10 Levels in Patients With Multiple System Atrophy.Semantic proximity Read ↗

Genome-wide association analysis identifies PLA2G4C as a susceptibility locus for Multiple System AtrophySemantic proximity Read ↗

Analysis of GWAS-linked variants in multiple system atrophy.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.