Long QT and Brugada syndromes: from genetics to clinical management

J Cardiovasc Electrophysiol. 2000 Oct;11(10):1174-8. doi: 10.1111/j.1540-8167.2000.tb01766.x.
No abstract available

MeSH terms

  • Arrhythmias, Cardiac / genetics*
  • Humans
  • KCNQ Potassium Channels
  • KCNQ1 Potassium Channel
  • Long QT Syndrome / genetics*
  • Long QT Syndrome / therapy
  • Mutation
  • NAV1.5 Voltage-Gated Sodium Channel
  • Phenotype
  • Potassium Channels / genetics*
  • Potassium Channels, Voltage-Gated*
  • Sodium Channels / genetics*
  • Syndrome

Substances

  • KCNQ Potassium Channels
  • KCNQ1 Potassium Channel
  • KCNQ1 protein, human
  • NAV1.5 Voltage-Gated Sodium Channel
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • SCN5A protein, human
  • Sodium Channels