Whole-exome sequencing identified novel KIF5A mutations in Chinese patients with amyotrophic lateral sclerosis and Charcot-Marie-Tooth type 2

J Neurol Neurosurg Psychiatry. 2020 Mar;91(3):326-328. doi: 10.1136/jnnp-2019-320483. Epub 2019 Aug 17.
No abstract available

Keywords: ALS; clinical neurology; genetics.

Publication types

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

MeSH terms

  • Amyotrophic Lateral Sclerosis / complications
  • Amyotrophic Lateral Sclerosis / genetics*
  • Asian People / genetics*
  • Charcot-Marie-Tooth Disease / complications
  • Charcot-Marie-Tooth Disease / genetics*
  • China
  • Exome Sequencing
  • Humans
  • Kinesins / genetics*
  • Mutation / genetics*

Substances

  • KIF5A protein, human
  • Kinesins