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

BRAIN (2014)

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Journal

BRAIN
Volume 137, Issue -, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/brain/awu265

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Clinical Neurology Neurosciences

Funding

  1. Intramural NIH HHS Funding Source: Medline
  2. NIA NIH HHS [Z01-AG000949-02] Funding Source: Medline

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