NEK1 mutations in familial amyotrophic lateral sclerosis

Brain. 2016 May;139(Pt 5):e28. doi: 10.1093/brain/aww033. Epub 2016 Mar 5.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Amyotrophic Lateral Sclerosis / complications
  • Amyotrophic Lateral Sclerosis / diagnostic imaging
  • Amyotrophic Lateral Sclerosis / genetics*
  • Brain / diagnostic imaging
  • Cohort Studies
  • Family Health*
  • Female
  • Gene Frequency
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Mutation / genetics*
  • NIMA-Related Kinase 1 / genetics*
  • Respiratory Insufficiency / etiology
  • Serine / genetics
  • Threonine / genetics

Substances

  • Threonine
  • Serine
  • NEK1 protein, human
  • NIMA-Related Kinase 1