Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2002-7-10
pubmed:abstractText
We sought to establish the role of genetic screening for ryanodine receptor type 2 (RyR2) gene mutations in families with effort-induced polymorphic ventricular arrhythmia (PVA), syncope and juvenile sudden death.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0735-1097
pubmed:author
pubmed:issnType
Print
pubmed:day
17
pubmed:volume
40
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
341-9
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:12106942-Adolescent, pubmed-meshheading:12106942-Adult, pubmed-meshheading:12106942-Child, pubmed-meshheading:12106942-Echocardiography, pubmed-meshheading:12106942-Electrocardiography, pubmed-meshheading:12106942-Electrocardiography, Ambulatory, pubmed-meshheading:12106942-Exercise Test, pubmed-meshheading:12106942-Female, pubmed-meshheading:12106942-Genetic Testing, pubmed-meshheading:12106942-Haplotypes, pubmed-meshheading:12106942-Heterozygote, pubmed-meshheading:12106942-Humans, pubmed-meshheading:12106942-Male, pubmed-meshheading:12106942-Middle Aged, pubmed-meshheading:12106942-Mutation, pubmed-meshheading:12106942-Pedigree, pubmed-meshheading:12106942-Ryanodine Receptor Calcium Release Channel, pubmed-meshheading:12106942-Signal Processing, Computer-Assisted, pubmed-meshheading:12106942-Syncope, pubmed-meshheading:12106942-Tachycardia, Ventricular
pubmed:year
2002
pubmed:articleTitle
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers.
pubmed:affiliation
Department of Cardiology, University of Padua Medical School, Via A. Gabelli, 86-35121 Padua, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't