Mechanisms of Disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
http://www.nature.com/articles/ncpcardio1182.pdf
Reference72 articles.
1. McKenna WJ et al. (1994) Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology. Br Heart J 71: 215–218
2. Uhl HS (1952) A previously undescribed congenital malformation of the heart: almost total absence of the myocardium of the right ventricle. Bull Johns Hopkins Hosp 91: 197–209
3. Gerlis LM et al. (1993) Dysplastic conditions of the right ventricular myocardium: Uhl's anomaly vs arrhythmogenic right ventricular dysplasia. Br Heart J 69: 142–150
4. Frank R et al. (1978) Electrocardiology of 4 cases of right ventricular dysplasia inducing arrhythmia [French]. Arch Mal Coeur Vaiss 71: 963–972
5. Nava A et al. (1987) A polymorphic form of familial arrhythmogenic right ventricular dysplasia. Am J Cardiol 59: 1405–1409
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