Inherited arrhythmia syndromes: exome sequencing opens a new door to diagnosis

J Am Coll Cardiol. 2014 Jan 28;63(3):267-8. doi: 10.1016/j.jacc.2013.07.089. Epub 2013 Sep 25.
No abstract available

Publication types

  • Editorial
  • Comment

MeSH terms

  • Calmodulin / genetics*
  • DNA / genetics*
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Monomeric Clathrin Assembly Proteins / genetics*
  • Mutation*
  • Ventricular Fibrillation / genetics*

Substances

  • Calmodulin
  • Monomeric Clathrin Assembly Proteins
  • PICALM protein, human
  • DNA