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Article

Genetic analysis of CHCHD10 in French familial amyotrophic lateral sclerosis patients.

Neurobiology of aging - 1 Jun 2016

Teyssou Elisa, Chartier Laura, Albert Mélanie, Bouscary Alexandra, Antoine Jean-Christophe, Camdessanché Jean-Philippe, Rotolo Francesco, Couratier Philippe, Salachas François, Seilhean Danielle, Millecamps Stéphanie

Abstract excerpt

Mutations in CHCHD10 have been reported as the cause of a large panel of neurologic disorders. To confirm the contribution of this gene to amyotrophic lateral sclerosis (ALS) disease, we analyzed the 4 coding exons of CHCHD10 by Sanger sequencing in a cohort of 118 French familial ALS already excluded for all known ALS-related genes. We did not find any pathogenic mutation suggesting that CHCHD10 is not a major...

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Source

Identifiers

PMID: 27095681
DOI: 10.1016/j.neurobiolaging.2016.03.022

Genes

CHCHD10

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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