Role of mutations in L-type calcium channel genes in Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation associated with right bundle branch block

Circ J. 2013;77(7):1689-90. doi: 10.1253/circj.cj-13-0641. Epub 2013 Jun 5.
No abstract available

Publication types

  • Editorial
  • Comment

MeSH terms

  • Calcium Channels, L-Type / genetics*
  • Female
  • Genetic Diseases, Inborn / genetics*
  • Humans
  • Male
  • Mutation*

Substances

  • CACNA1C protein, human
  • Calcium Channels, L-Type