Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

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Bibliographic Details
Published in:	Brain
Main Authors:	Johnson, Janel O., Glynn, Shannon M., Gibbs, J. Raphael, Nalls, Mike A., Sabatelli, Mario, Restagno, Gabriella, Drory, Vivian E., Chiò, Adriano, Rogaeva, Ekaterina, Traynor, Bryan J.
Format:	Artigo
Language:	Inglês
Published:	Oxford University Press 2014
Subjects:	Letters to the Editor
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC4240285/ https://ncbi.nlm.nih.gov/pubmed/25261972 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awu265
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