Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotype

Eur Heart J. 2007 Mar;28(5):529-30. doi: 10.1093/eurheartj/ehl530. Epub 2007 Feb 15.
No abstract available

Publication types

  • Comment
  • Editorial

MeSH terms

  • Arrhythmogenic Right Ventricular Dysplasia / genetics*
  • Cardiomyopathies
  • Desmoglein 2 / genetics*
  • Genotype
  • Humans
  • Mutation / genetics*
  • Phenotype

Substances

  • Desmoglein 2