Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotype
- PMID: 17303588
- DOI: 10.1093/eurheartj/ehl530
Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotype
Comment on
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Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease.Eur Heart J. 2007 Mar;28(5):581-8. doi: 10.1093/eurheartj/ehl380. Epub 2006 Nov 14. Eur Heart J. 2007. PMID: 17105751
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