Ion channel mechanisms related to sudden cardiac death in phenotype-negative long-QT syndrome genotype-phenotype correlations of the KCNQ1(S349W) mutation

J Cardiovasc Electrophysiol. 2011 Feb;22(2):193-200. doi: 10.1111/j.1540-8167.2010.01852.x.
No abstract available

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Child
  • Death, Sudden, Cardiac*
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Humans
  • Ion Channel Gating / genetics*
  • KCNQ1 Potassium Channel / genetics*
  • Long QT Syndrome / genetics*
  • Male
  • Phenotype
  • Polymorphism, Single Nucleotide

Substances

  • KCNQ1 Potassium Channel
  • KCNQ1 protein, human