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

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

Research output: Contribution to journalArticle

86 Citations (Scopus)

Abstract

n/a
Original languageEnglish
Pages (from-to)e311-e311
JournalBRAIN
Volume137
DOIs
Publication statusPublished - 2014

Keywords

  • Amyotrophic Lateral Sclerosis
  • DNA, Mitochondrial
  • Female
  • Frontotemporal Dementia
  • Humans
  • Male
  • Mitochondria
  • Mitochondrial Diseases
  • Mitochondrial Proteins

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