C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia

Mov Disord. 2012 Dec;27(14):1832-3. doi: 10.1002/mds.25245. Epub 2012 Oct 18.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Amyotrophic Lateral Sclerosis / genetics*
  • C9orf72 Protein
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Proteins / genetics*
  • Spinocerebellar Ataxias / diagnosis
  • Spinocerebellar Ataxias / genetics*

Substances

  • C9orf72 Protein
  • C9orf72 protein, human
  • Proteins