rdf:type |
|
lifeskim:mentions |
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pubmed:issue |
19
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pubmed:dateCreated |
2003-5-8
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pubmed:abstractText |
Mutations in potassium-channel genes KCNQ1 (LQT1 locus) and KCNH2 (LQT2 locus) and the sodium-channel gene SCN5A (LQT3 locus) are the most common causes of the long-QT syndrome. We stratified risk according to the genotype, in conjunction with other clinical variables such as sex and the length of the QT interval.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
1533-4406
|
pubmed:author |
pubmed-author:BloiseRaffaellaR,
pubmed-author:BottelliGeorgiaG,
pubmed-author:CappellettiDonataD,
pubmed-author:FolliRobertaR,
pubmed-author:GrilloMassimilianoM,
pubmed-author:NapolitanoCarloC,
pubmed-author:NastoliJanniJ,
pubmed-author:PrioriSilvia GSG,
pubmed-author:RonchettiElenaE,
pubmed-author:SchwartzPeter JPJ,
pubmed-author:SpazzoliniCarlaC,
pubmed-author:VicentiniAlessandroA
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pubmed:copyrightInfo |
Copyright 2003 Massachusetts Medical Society
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pubmed:issnType |
Electronic
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pubmed:day |
8
|
pubmed:volume |
348
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
1866-74
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12736279-Adult,
pubmed-meshheading:12736279-Age of Onset,
pubmed-meshheading:12736279-Disease-Free Survival,
pubmed-meshheading:12736279-Electrocardiography,
pubmed-meshheading:12736279-Female,
pubmed-meshheading:12736279-Genotype,
pubmed-meshheading:12736279-Heart Arrest,
pubmed-meshheading:12736279-Humans,
pubmed-meshheading:12736279-Long QT Syndrome,
pubmed-meshheading:12736279-Male,
pubmed-meshheading:12736279-Multivariate Analysis,
pubmed-meshheading:12736279-Mutation,
pubmed-meshheading:12736279-Phenotype,
pubmed-meshheading:12736279-Potassium Channels,
pubmed-meshheading:12736279-Risk Assessment,
pubmed-meshheading:12736279-Sodium Channels
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pubmed:year |
2003
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pubmed:articleTitle |
Risk stratification in the long-QT syndrome.
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pubmed:affiliation |
Department of Molecular Cardiology, Istituto di Ricovero e Cura a Carattere Scientifico Fondazione S. Maugeri, University of Pavia, Pavia, Italy. spriori@fsm.it.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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