Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with the long QT syndrome

This publication has 23 references indexed in Scilit:

• A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
  Nature Genetics, 1997
• 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
• Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
  Nature Genetics, 1994
• Left cardiac sympathetic denervation in the therapy of congenital long QT syndrome. A worldwide report.
  Circulation, 1991
• Linkage of a Cardiac Arrhythmia, the Long QT Syndrome, and the Harvey ras -1 Gene
  Science, 1991
• Prolonged QT-Interval Syndromes
  Published by American Medical Association (AMA) ,1986
• The long Q-T syndrome
  American Heart Journal, 1975
• Unilateral Cervicothoracic Sympathetic Ganglionectomy for the Treatment of Long QT Interval Syndrome
  New England Journal of Medicine, 1971