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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2010-12-27
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pubmed:abstractText |
The aim of this study was to investigate, in a set of 93 mutation-negative long QT syndrome (LQTS) probands, the frequency of copy number variants (CNVs) in LQTS genes.
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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 |
1558-3597
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pubmed:author |
pubmed-author:BarcJulienJ,
pubmed-author:BaronEstelleE,
pubmed-author:BriecFrançoisF,
pubmed-author:KyndtFlorenceF,
pubmed-author:Le CaignecCédricC,
pubmed-author:Le CunffMartineM,
pubmed-author:Le MarecHervéH,
pubmed-author:ProbstVincentV,
pubmed-author:RedonRichardR,
pubmed-author:SacherFrédéricF,
pubmed-author:SchmittSébastienS,
pubmed-author:SchottJean-JacquesJJ,
pubmed-author:VieyresClaudeC
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pubmed:copyrightInfo |
Copyright © 2011 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
4
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pubmed:volume |
57
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
40-7
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pubmed:dateRevised |
2011-7-22
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pubmed:meshHeading |
pubmed-meshheading:21185499-Adolescent,
pubmed-meshheading:21185499-Adult,
pubmed-meshheading:21185499-Aged,
pubmed-meshheading:21185499-Child,
pubmed-meshheading:21185499-DNA,
pubmed-meshheading:21185499-Electrocardiography,
pubmed-meshheading:21185499-Ether-A-Go-Go Potassium Channels,
pubmed-meshheading:21185499-Female,
pubmed-meshheading:21185499-Genetic Linkage,
pubmed-meshheading:21185499-Genetic Testing,
pubmed-meshheading:21185499-Genetic Variation,
pubmed-meshheading:21185499-Humans,
pubmed-meshheading:21185499-KCNQ1 Potassium Channel,
pubmed-meshheading:21185499-Long QT Syndrome,
pubmed-meshheading:21185499-Male,
pubmed-meshheading:21185499-Middle Aged,
pubmed-meshheading:21185499-Muscle Proteins,
pubmed-meshheading:21185499-Pedigree,
pubmed-meshheading:21185499-Point Mutation,
pubmed-meshheading:21185499-Polymerase Chain Reaction,
pubmed-meshheading:21185499-Sodium Channels,
pubmed-meshheading:21185499-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
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pubmed:affiliation |
INSERM, UMR915, l'institut du thorax, Service de cardiologie Nantes, Nantes, France.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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