Identification of two new KCNA1 mutations in episodic ataxia/myokymia families

Hum Mol Genet. 1995 Sep;4(9):1671-2. doi: 10.1093/hmg/4.9.1671.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Ataxia / genetics*
  • Base Sequence
  • DNA
  • Fasciculation / genetics*
  • Female
  • Humans
  • Kv1.1 Potassium Channel
  • Male
  • Molecular Sequence Data
  • Pedigree
  • Point Mutation*
  • Potassium Channels / genetics*
  • Potassium Channels, Voltage-Gated*

Substances

  • KCNA1 protein, human
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Kv1.1 Potassium Channel
  • DNA