Mechanisms of Disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy

被引：0
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作者：
Mark M Awad
Hugh Calkins
Daniel P Judge
机构：
[1] MM Awad is an MD-PhD Candidate at the Johns Hopkins University School of Medicine and the Johns Hopkins University Cellular and Molecular Medicine program,
[2] Baltimore,undefined
[3] MD,undefined
[4] USA.,undefined
[5] H Calkins is a Professor of Medicine at the Johns Hopkins University School of Medicine and Director of the Electrophysiology Laboratory at the Johns Hopkins Hospital,undefined
[6] Baltimore,undefined
[7] MD,undefined
[8] USA.,undefined
[9] DP Judge is Assistant Professor of Medicine at the Johns Hopkins University School of Medicine and Medical Director of the Center for Inherited Heart Disease at Johns Hopkins Hospital,undefined
[10] Baltimore,undefined
[11] MD,undefined
[12] USA.,undefined
来源：
Nature Clinical Practice Cardiovascular Medicine | 2008年 / 5卷
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摘要：
Here, Mark Awad, Hugh Calkins and Daniel Judge tackle the known genetic mutations associated with arrhythmogenic right ventricular dysplasia/cardiomyopathy, and examine the complex issues surrounding genetic analysis in the clinical assessment of individuals with this condition.
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页码：258 / 267
页数：9
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