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Article

Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy.

CNS neuroscience & therapeutics - 1 Aug 2015

Wen Xiao-Dan, Li Hong-Fu, Wang Hong-Xia, Ni Wang, Dong Yi, Wu Zhi-Ying

Abstract excerpt

AIMS: Recently, mutations in COQ2 encoding para-hydroxybenzoate-polyprenyl transferase have been identified to increase the risk of multiple system atrophy (MSA) in multiplex families and sporadic cases. The prevalence of COQ2 mutations was showed to be higher in cerebellar subtype (MSA-C) than parkinsonism subtype (MSA-P). The aim of this study was to investigate the association between COQ2 mutations and MSA-C...

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Source

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Identifiers

PMID: 26096180
DOI: 10.1111/cns.12412
PMCID: PMC6495228

Genes

COQ2

Variants

Provenance

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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