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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2010-8-18
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pubmed:abstractText |
Isolated cardiac conduction block is a relatively common condition in young and elderly populations. Genetic predisposing factors have long been suspected because of numerous familial case reports. Deciphering genetic predisposing factors of conduction blocks may give a hint at stratifying conduction block carriers in a more efficient way.
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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 |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1942-3268
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pubmed:author |
pubmed-author:BeckmannAlfA,
pubmed-author:BlaysatGérardG,
pubmed-author:BouvagnetPatriceP,
pubmed-author:BozioAndréA,
pubmed-author:El ZeinLoubnaL,
pubmed-author:GuinamardRomainR,
pubmed-author:KUOH YHY,
pubmed-author:KruseMartinM,
pubmed-author:KurtbayGüvenG,
pubmed-author:MégarbanéAndréA,
pubmed-author:OhmertIrisI,
pubmed-author:PongsOlafO,
pubmed-author:VillainElisabethE
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pubmed:issnType |
Electronic
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
374-85
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pubmed:meshHeading |
pubmed-meshheading:20562447-Animals,
pubmed-meshheading:20562447-CHO Cells,
pubmed-meshheading:20562447-COS Cells,
pubmed-meshheading:20562447-Cells, Cultured,
pubmed-meshheading:20562447-Cercopithecus aethiops,
pubmed-meshheading:20562447-Cricetinae,
pubmed-meshheading:20562447-Cricetulus,
pubmed-meshheading:20562447-Family,
pubmed-meshheading:20562447-Female,
pubmed-meshheading:20562447-Genes, Dominant,
pubmed-meshheading:20562447-Genetic Linkage,
pubmed-meshheading:20562447-Heart Block,
pubmed-meshheading:20562447-Humans,
pubmed-meshheading:20562447-Male,
pubmed-meshheading:20562447-Mutation,
pubmed-meshheading:20562447-Pedigree,
pubmed-meshheading:20562447-TRPM Cation Channels,
pubmed-meshheading:20562447-Transfection
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pubmed:year |
2010
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pubmed:articleTitle |
Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease.
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pubmed:affiliation |
Université de Lyon, Laboratoire Cardiogénétique, Equipe d'Accueil 4171, Lyon, France.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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