Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis

J Neurol Neurosurg Psychiatry. 2016 Nov;87(11):1272-1274. doi: 10.1136/jnnp-2016-313337. Epub 2016 Jun 16.
No abstract available

Keywords: ALS; NEUROGENETICS.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyotrophic Lateral Sclerosis / genetics*
  • Asian People / genetics*
  • Ataxin-2 / genetics
  • C9orf72 Protein / genetics
  • Female
  • Humans
  • Male
  • Mutation / genetics*

Substances

  • ATXN2 protein, human
  • Ataxin-2
  • C9orf72 Protein
  • C9orf72 protein, human