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

✍ Scribed by Johnson, J. O.; Glynn, S. M.; Gibbs, J. R.; Nalls, M. A.; Sabatelli, M.; Restagno, G.; Drory, V. E.; Chio, A.; Rogaeva, E.; Traynor, B. J.

Book ID: 126910517
Publisher: Oxford University Press
Year: 2014
Tongue: English
Weight: 82 KB
Volume: 137
Category: Article
ISSN: 0006-8950
DOI: 10.1093/brain/awu265

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