Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)

This publication has 28 references indexed in Scilit:

• Mutations in the hminK gene cause long QT syndrome and suppress lKs function
  Nature Genetics, 1997
• Multiple Mechanisms in the Long-QT Syndrome
  Circulation, 1996
• The roles of ion channels in an inherited heart disease: molecular genetics of the long QT syndrome
  Cardiovascular Research, 1996
• Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
  Nature Genetics, 1996
• SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
  Cell, 1995
• A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
  Cell, 1995
• Auditory Stimuli as a Major Cause of Syncope in a Patient with Idiopathic Long QT Syndrome.
  Japanese Circulation Journal, 1995
• Epinephrine‐Induced Ventricular Premature Complexes Due to Early Afterdepolarizations and Effects of Verapamil and Propranolol in a Patient with Congenital Long QT Syndrome
  Journal of Cardiovascular Electrophysiology, 1994
• Linkage of a Cardiac Arrhythmia, the Long QT Syndrome, and the Harvey ras -1 Gene
  Science, 1991
• Ventricular Fibrillation Occurring on Arousal from Sleep by Auditory Stimuli
  Circulation, 1972