Is restoration of intracellular trafficking clinically feasible in the long QT syndrome?: The example of HERG mutations

J Cardiovasc Electrophysiol. 2003 Mar;14(3):320-2. doi: 10.1046/j.1540-8167.2003.02363.x.
No abstract available

Publication types

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

MeSH terms

  • Biological Transport
  • Cation Transport Proteins*
  • DNA-Binding Proteins*
  • ERG1 Potassium Channel
  • Ether-A-Go-Go Potassium Channels
  • Forecasting
  • Humans
  • Long QT Syndrome / genetics*
  • Long QT Syndrome / physiopathology
  • Mutation, Missense
  • Potassium Channels / genetics*
  • Potassium Channels, Voltage-Gated*
  • Trans-Activators*
  • Transcriptional Regulator ERG

Substances

  • Cation Transport Proteins
  • DNA-Binding Proteins
  • ERG protein, human
  • ERG1 Potassium Channel
  • Ether-A-Go-Go Potassium Channels
  • KCNH2 protein, human
  • KCNH6 protein, human
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Trans-Activators
  • Transcriptional Regulator ERG