Episodic ataxia: SLC1A3 and CACNB4 do not explain the apparent genetic heterogeneity

J Neurol. 2008 Jul;255(7):1097-9. doi: 10.1007/s00415-008-0844-4. Epub 2008 May 2.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Ataxia / genetics*
  • Calcium Channels / genetics*
  • Child
  • DNA Mutational Analysis
  • Excitatory Amino Acid Transporter 1 / genetics*
  • Family Health
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mutation / genetics*

Substances

  • CACNB4 protein, human
  • Calcium Channels
  • Excitatory Amino Acid Transporter 1
  • SLC1A3 protein, human