CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis

J Neurol Neurosurg Psychiatry. 2008 Jul;79(7):849-50. doi: 10.1136/jnnp.2007.140541. Epub 2008 Feb 12.
No abstract available

Publication types

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

MeSH terms

  • Amyotrophic Lateral Sclerosis / ethnology
  • Amyotrophic Lateral Sclerosis / genetics*
  • Australia
  • Cohort Studies
  • Endosomal Sorting Complexes Required for Transport
  • Humans
  • Mutation / genetics*
  • Nerve Tissue Proteins / genetics*
  • Polymorphism, Single Nucleotide / genetics
  • United Kingdom
  • White People / genetics*

Substances

  • CHMP2B protein, human
  • Endosomal Sorting Complexes Required for Transport
  • Nerve Tissue Proteins