Clinical and genetic features of spinocerebellar ataxia type 8

Handb Clin Neurol. 2012:103:493-505. doi: 10.1016/B978-0-444-51892-7.00031-0.
No abstract available

Publication types

  • Review

MeSH terms

  • Animals
  • Brain / pathology
  • Family Health
  • Female
  • Humans
  • Magnetic Resonance Imaging / methods
  • Male
  • Mice
  • Nerve Tissue Proteins / genetics*
  • Spinocerebellar Degenerations / diagnosis*
  • Spinocerebellar Degenerations / genetics*
  • Trinucleotide Repeat Expansion / genetics*

Substances

  • ATXN8 protein, human
  • Nerve Tissue Proteins

Supplementary concepts

  • Spinocerebellar ataxia 8