Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy

Ann N Y Acad Sci. 1999 Apr 30;868:442-6. doi: 10.1111/j.1749-6632.1999.tb11310.x.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ataxia / genetics*
  • Cloning, Molecular
  • Epilepsy / genetics*
  • Humans
  • Kv1.1 Potassium Channel
  • Microinjections
  • Mutation
  • Oocytes / metabolism
  • Patch-Clamp Techniques
  • Potassium Channels / genetics*
  • Potassium Channels, Voltage-Gated*
  • RNA, Messenger / genetics
  • Xenopus laevis

Substances

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