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Article

Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease.

Neurobiology of aging - 1 Feb 2016

Zhang Ming, Xi Zhengrui, Fang Shilun, Ghani Mahdi, Sato Christine, Moreno Danielle, Liang Yan, Lang Anthony E, Rogaeva Ekaterina

Abstract excerpt

Recently, several CHCHD2 mutations were reported to be associated with autosomal dominant Parkinson's disease (PD) in a Japanese population. However, an association between CHCHD2 and PD was not observed in 2 Caucasian data sets. The present study searched for CHCHD2 coding variants in Canadian PD patients. Sanger sequencing of all CHCHD2 exons revealed no coding mutations in 155 familial cases. Moreover, 3...

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Source

Identifiers

PMID: 26639156
DOI: 10.1016/j.neurobiolaging.2015.10.038

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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