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Familial Evaluation in Arrhythmogenic Right Ventricular Cardiomyopathy
Author(s) -
Giovanni Quarta,
Alison Muir,
Antonios Pantazis,
Petros Syrris,
Katja Gehmlich,
Pablo GarcíaPavía,
Deirdre Ward,
Srijita SenChowdhry,
Perry Elliott,
William J. McKenna
Publication year - 2011
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.110.976936
Subject(s) - penetrance , medicine , proband , arrhythmogenic right ventricular dysplasia , cardiomyopathy , odds ratio , cardiology , disease , expressivity , heart disease , pedigree chart , genetic heterogeneity , genetics , mutation , phenotype , heart failure , gene , biology
With recognition of disease-causing genes in arrhythmogenic right ventricular cardiomyopathy, mutation analysis is being applied.

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