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

120 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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