Novel mutation in the KCNH2 gene associated with long QT syndrome

Rev Port Cardiol. 2013 Feb;32(2):163-4. doi: 10.1016/j.repc.2012.06.012. Epub 2013 Jan 23.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • ERG1 Potassium Channel
  • Ether-A-Go-Go Potassium Channels / genetics*
  • Humans
  • Long QT Syndrome / genetics*
  • Male
  • Mutation*

Substances

  • ERG1 Potassium Channel
  • Ether-A-Go-Go Potassium Channels
  • KCNH2 protein, human