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

Janel O. Johnson, Shannon M. Glynn, J. Raphael Gibbs, Mike A. Nalls, Mario Sabatelli, Gabriella Restagno, Vivian E. Drory, Adriano Chiò, Ekaterina Rogaeva, Bryan J. Traynor*

*Corresponding author for this work

Research output: Contribution to journalLetterpeer-review

114 Scopus citations
Original languageEnglish
Pages (from-to)e311
JournalBrain
Volume137
Issue number12
DOIs
StatePublished - 1 Dec 2014
Externally publishedYes

Funding

FundersFunder number
National Institute on AgingZ01AG000949, ZIAAG000933
Seventh Framework Programme259867
European Commission278611

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