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

Tools

Item Type:	Letter
Title:	Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy
Creators Name:	Posch, M.G., Posch, M.J., Perrot, A., Dietz, R. and Oezcelik, C.
Abstract:	Arising from: Awad MM et al. (2008) Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Nat Clin Pract Cardiovasc Med 5: 258–267 doi: 10.1038/ncpcardio1182
Keywords:	Arrhythmogenic Right Ventricular Dysplasia, Dilated Cardiomyopathy, Case-Control Studies, Desmocollins, Desmoglein 2, Gene Frequency, Genetic Predisposition to Disease, Genetic Polymorphism, Risk Factors
Source:	Nature Clinical Practice Cardiovascular Medicine
ISSN:	1743-4297
Publisher:	Nature Publishing Group
Volume:	5
Number:	12
Page Range:	E1
Date:	December 2008
Official Publication:	https://doi.org/10.1038/ncpcardio1434
PubMed:	View item in PubMed

Repository Staff Only: item control page