Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome

This publication has 27 references indexed in Scilit:

• SCN4B -Encoded Sodium Channel β4 Subunit in Congenital Long-QT Syndrome
  Circulation, 2007
• Genetic Testing in the Long QT Syndrome
  JAMA, 2005
• The congenital long QT syndromes from genotype to phenotype: clinical implications
  Journal of Internal Medicine, 2005
• Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing
  Heart Rhythm, 2005
• Genotype-Phenotype Correlation in the Long-QT Syndrome
  Circulation, 2001
• Spectrum of Mutations in Long-QT Syndrome Genes
  Circulation, 2000
• Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)
  Journal of the American College of Cardiology, 1999
• Ion Channels — Basic Science and Clinical Disease
  New England Journal of Medicine, 1997
• The Spectrum of Symptoms and QT Intervals in Carriers of the Gene for the Long-QT Syndrome
  New England Journal of Medicine, 1992
• The long QT syndrome. Prospective longitudinal study of 328 families.
  Circulation, 1991