Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy

Nat Clin Pract Cardiovasc Med. 2008 Dec;5(12):E1. doi: 10.1038/ncpcardio1434.
No abstract available

Publication types

  • Comment

MeSH terms

  • Arrhythmogenic Right Ventricular Dysplasia / genetics*
  • Cardiomyopathy, Dilated / genetics*
  • Case-Control Studies
  • Desmocollins / genetics*
  • Desmoglein 2 / genetics*
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Humans
  • Polymorphism, Genetic*
  • Risk Factors

Substances

  • DSC2 protein, human
  • DSG2 protein, human
  • Desmocollins
  • Desmoglein 2