Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: Impact of genetics and revised task force criteria

Circulation

Volumn 123, Issue 23, 2011, Pages 2701-2709

  Quarta, Giovanni ^a,b   Muir, Alison ^a   Pantazis, Antonios ^a   Syrris, Petros ^c   Gehmlich, Katja ^c   Garcia Pavia, Pablo ^a   Ward, Deirdre ^a   Sen Chowdhry, Srijita ^a,c,d   Elliott, Perry M ^a,c   McKenna, William J ^a,c  

^a UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d IMPERIAL COLLEGE LONDON   (United Kingdom)

Author keywords

arrhythmogenic right ventricular cardiomyopathy; desmosomes; family; genes

Indexed keywords

ADULT; ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; FAMILIAL INCIDENCE; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC VARIABILITY; GENOTYPE; HEART RIGHT VENTRICLE DYSPLASIA; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL;

ADULT; ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA; DESMOSOMES; ELECTROCARDIOGRAPHY; FAMILY; FEMALE; FOLLOW-UP STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; PEDIGREE; PENETRANCE; POINT MUTATION; PREVALENCE; RISK FACTORS; TACHYCARDIA, VENTRICULAR;

EID: 79959569308     PISSN: 00097322     EISSN: 15244539     Source Type: Journal    
DOI: 10.1161/CIRCULATIONAHA.110.976936     Document Type: Article

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