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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2007-1-23
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pubmed:abstractText |
The hypothesis that some cases of sudden infant death syndrome (SIDS) could be caused by long-QT syndrome (LQTS) has been supported by molecular studies. However, there are inadequate data regarding the true prevalence of mutations in arrhythmia-susceptibility genes among SIDS cases. Given the importance and potential implications of these observations, we performed a study to more accurately quantify the contribution to SIDS of LQTS gene mutations and rare variants.
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pubmed:grant |
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1524-4539
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pubmed:author |
pubmed-author:ArnestadMarianneM,
pubmed-author:CrottiLiaL,
pubmed-author:FerrandiChiaraC,
pubmed-author:GeorgeAlfred LALJr,
pubmed-author:InsoliaRobertoR,
pubmed-author:PedrazziniMatteoM,
pubmed-author:RhodesTroy ETE,
pubmed-author:RognumTorleiv OTO,
pubmed-author:SchwartzPeter JPJ,
pubmed-author:VegeAshildA,
pubmed-author:WangDao WDW
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pubmed:issnType |
Electronic
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pubmed:day |
23
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pubmed:volume |
115
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
361-7
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pubmed:dateRevised |
2011-7-22
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pubmed:meshHeading |
pubmed-meshheading:17210839-Adult,
pubmed-meshheading:17210839-Arrhythmias, Cardiac,
pubmed-meshheading:17210839-Case-Control Studies,
pubmed-meshheading:17210839-Caveolin 3,
pubmed-meshheading:17210839-Child, Preschool,
pubmed-meshheading:17210839-Electrocardiography,
pubmed-meshheading:17210839-Female,
pubmed-meshheading:17210839-Genetic Testing,
pubmed-meshheading:17210839-Genetic Variation,
pubmed-meshheading:17210839-Humans,
pubmed-meshheading:17210839-Infant,
pubmed-meshheading:17210839-Long QT Syndrome,
pubmed-meshheading:17210839-Male,
pubmed-meshheading:17210839-Middle Aged,
pubmed-meshheading:17210839-Muscle Proteins,
pubmed-meshheading:17210839-Mutation,
pubmed-meshheading:17210839-Norway,
pubmed-meshheading:17210839-Potassium Channels,
pubmed-meshheading:17210839-Risk Factors,
pubmed-meshheading:17210839-Single-Blind Method,
pubmed-meshheading:17210839-Sodium Channels,
pubmed-meshheading:17210839-Sudden Infant Death
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pubmed:year |
2007
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pubmed:articleTitle |
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
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pubmed:affiliation |
Institute of Forensic Medicine, University of Oslo, Oslo, Norway.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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