Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies

This publication has 45 references indexed in Scilit:

• Clinical Aspects of Type-1 Long-QT Syndrome by Location, Coding Type, and Biophysical Function of Mutations Involving the KCNQ1 Gene
  Circulation, 2007
• Sodium channel kinetic changes that produce Brugada syndrome or progressive cardiac conduction system disease
  American Journal of Physiology-Heart and Circulatory Physiology, 2007
• A sodium channel pore mutation causing Brugada syndrome
  Heart Rhythm, 2007
• Genetic and biophysical basis for bupivacaine-induced ST segment elevation and VT/VF. Anesthesia unmasked Brugada syndrome
  Heart Rhythm, 2006
• Brugada syndrome and fever: Genetic and molecular characterization of patients carrying mutations
  Cardiovascular Research, 2005
• A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families
  Journal of Molecular and Cellular Cardiology, 2005
• Delay in Right Ventricular Activation Contributes to Brugada Syndrome
  Circulation, 2004
• Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease
  JACC, 2003
• Proposed Diagnostic Criteria for the Brugada Syndrome
  European Heart Journal, 2002
• The Vulnerable Window for Unidirectional Block in Cardiac Tissue:
  Journal of Cardiovascular Electrophysiology, 1995