Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria-Reference-Cited by-同舟云学术

Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria

Published:2002-10 Issue:8 Volume:40 Page:1445-1450
ISSN:0735-1097
Container-title:Journal of the American College of Cardiology
language:en
Short-container-title:Journal of the American College of Cardiology

Author:

Hamid M.Shoaib,Norman Mark,Quraishi Asifa,Firoozi Sami,Thaman Rajesh,Gimeno Juan R,Sachdev Bhavesh,Rowland Edward,Elliott Perry M,McKenna William J

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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4. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2);Tiso;Hum Mol Genet,2001

5. 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.

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