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

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

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