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Article

Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis.

Journal of the neurological sciences - 15 Sept 2016

Yang Xinglong, An Ran, Zhao Quanzhen, Zheng Jinhua, Tian Sijia, Chen Yalan, Xu Yanming

Abstract excerpt

CHCHD2, which encodes a regulator of mitochondrial metabolism, has been linked to Parkinson's disease (PD) in a Japanese population. Since PD and two other neurodegenerative diseases, multiple system atrophy (MSA) and amyotrophic lateral sclerosis (ALS), are associated with mitochondrial dysfunction, we wanted to know whether CHCHD2 mutations may be linked to MSA and sporadic ALS in Chinese patients. All four...

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Source

Identifiers

PMID: 27538669
DOI: 10.1016/j.jns.2016.07.063

Genes

CHCHD2

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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