17222736

Source:http://linkedlifedata.com/resource/pubmed/id/17222736

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004398, umls-concept:C0011065, umls-concept:C0023976, umls-concept:C0679560, umls-concept:C1276802
pubmed:issue	2
pubmed:dateCreated	2007-1-15
pubmed:abstractText	This study sought to determine the spectrum and prevalence of long QT syndrome (LQTS)-associated mutations in a large cohort of autopsy-negative sudden unexplained death (SUD).
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/17222736-17222737
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8301365
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/KCNQ1 Potassium Channel, http://linkedlifedata.com/resource/pubmed/chemical/KCNQ1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Ryanodine Receptor Calcium Release...
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1558-3597
pubmed:author	pubmed-author:AckermanMichael JMJ, pubmed-author:TesterDavid JDJ
pubmed:issnType	Electronic
pubmed:day	16
pubmed:volume	49
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	240-6
pubmed:meshHeading	pubmed-meshheading:17222736-Adolescent, pubmed-meshheading:17222736-Adult, pubmed-meshheading:17222736-Age Distribution, pubmed-meshheading:17222736-Autopsy, pubmed-meshheading:17222736-Causality, pubmed-meshheading:17222736-Cause of Death, pubmed-meshheading:17222736-Child, pubmed-meshheading:17222736-Cohort Studies, pubmed-meshheading:17222736-Confidence Intervals, pubmed-meshheading:17222736-DNA Mutational Analysis, pubmed-meshheading:17222736-Death, Sudden, pubmed-meshheading:17222736-Death, Sudden, Cardiac, pubmed-meshheading:17222736-Diagnosis, pubmed-meshheading:17222736-Female, pubmed-meshheading:17222736-Genetic Predisposition to Disease, pubmed-meshheading:17222736-Humans, pubmed-meshheading:17222736-KCNQ1 Potassium Channel, pubmed-meshheading:17222736-Long QT Syndrome, pubmed-meshheading:17222736-Male, pubmed-meshheading:17222736-Mutation, pubmed-meshheading:17222736-Polymorphism, Genetic, pubmed-meshheading:17222736-Retrospective Studies, pubmed-meshheading:17222736-Ryanodine Receptor Calcium Release Channel, pubmed-meshheading:17222736-Sensitivity and Specificity, pubmed-meshheading:17222736-Sex Distribution
pubmed:year	2007
pubmed:articleTitle	Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.
pubmed:affiliation	Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, Minnesota 55905-0001, USA.
pubmed:publicationType	Journal Article