A de novo SCA14 mutation in an isolated case of late-onset cerebellar ataxia

Mov Disord. 2013 Nov;28(13):1902-3. doi: 10.1002/mds.25572. Epub 2013 Jul 12.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Humans
  • Male
  • Middle Aged
  • Protein Kinase C / genetics*
  • Spinocerebellar Ataxias
  • Spinocerebellar Degenerations / genetics*

Substances

  • protein kinase C gamma
  • Protein Kinase C

Supplementary concepts

  • Spinocerebellar ataxia 14