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

Abstract:

BACKGROUND: With recognition of disease-causing genes in arrhythmogenic right ventricular cardiomyopathy, mutation analysis is being applied. METHODS AND RESULTS: The role of genotyping in familial assessment for arrhythmogenic right ventricular cardiomyopathy was investigated, including the prevalence of mutations in known causal genes, the penetrance and expressivity in genotyped families, and the utility of the 2010 Task Force criteria in clinical diagnosis. Clinical and molecular genetic...

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Authors


Pantazis, A More by this author
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Institution:
University of Oxford
Department:
Oxford, MSD, RDM, Cardiovascular Medicine, BHF Centre of Research Excellence
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Journal:
Circulation
Volume:
123
Issue:
23
Pages:
2701-2709
Publication date:
2011-06-05
DOI:
EISSN:
1524-4539
ISSN:
0009-7322
URN:
uuid:7ded0bd0-50f6-4dd0-b25a-99f39bc2e0c7
Source identifiers:
269715
Local pid:
pubs:269715

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