rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
23
|
pubmed:dateCreated |
2011-6-14
|
pubmed:abstractText |
With recognition of disease-causing genes in arrhythmogenic right ventricular cardiomyopathy, mutation analysis is being applied.
|
pubmed:grant |
|
pubmed:commentsCorrections |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
1524-4539
|
pubmed:author |
|
pubmed:issnType |
Electronic
|
pubmed:day |
14
|
pubmed:volume |
123
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2701-9
|
pubmed:meshHeading |
pubmed-meshheading:21606390-Adult,
pubmed-meshheading:21606390-Arrhythmogenic Right Ventricular Dysplasia,
pubmed-meshheading:21606390-Desmosomes,
pubmed-meshheading:21606390-Electrocardiography,
pubmed-meshheading:21606390-Family,
pubmed-meshheading:21606390-Female,
pubmed-meshheading:21606390-Follow-Up Studies,
pubmed-meshheading:21606390-Genetic Predisposition to Disease,
pubmed-meshheading:21606390-Genotype,
pubmed-meshheading:21606390-Humans,
pubmed-meshheading:21606390-Male,
pubmed-meshheading:21606390-Middle Aged,
pubmed-meshheading:21606390-Pedigree,
pubmed-meshheading:21606390-Penetrance,
pubmed-meshheading:21606390-Point Mutation,
pubmed-meshheading:21606390-Prevalence,
pubmed-meshheading:21606390-Risk Factors,
pubmed-meshheading:21606390-Tachycardia, Ventricular
|
pubmed:year |
2011
|
pubmed:articleTitle |
Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteria.
|
pubmed:affiliation |
Heart Hospital, University College London Hospitals Trust, London, UK.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|