SCN5A mutation associated with ventricular fibrillation, early repolarization, and concealed myocardial abnormalities

Int J Cardiol. 2013 May 10;165(2):e21-3. doi: 10.1016/j.ijcard.2012.10.074. Epub 2012 Nov 17.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Review

MeSH terms

  • Adult
  • Humans
  • Male
  • Mutation, Missense / genetics*
  • Myocardium / pathology
  • NAV1.5 Voltage-Gated Sodium Channel / genetics*
  • Time Factors
  • Ventricular Fibrillation / diagnosis
  • Ventricular Fibrillation / genetics*

Substances

  • NAV1.5 Voltage-Gated Sodium Channel
  • SCN5A protein, human