pubmed-article:17984373 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C0015031 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C0035647 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C0015127 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C0205082 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C1416612 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C1514983 | lld:lifeskim |
pubmed-article:17984373 | lifeskim:mentions | umls-concept:C0205214 | lld:lifeskim |
pubmed-article:17984373 | pubmed:issue | 21 | lld:pubmed |
pubmed-article:17984373 | pubmed:dateCreated | 2007-11-20 | lld:pubmed |
pubmed-article:17984373 | pubmed:abstractText | The impressive clinical heterogeneity of the long-QT syndrome (LQTS) remains partially unexplained. In a South African (SA) founder population, we identified a common LQTS type 1 (LQT1)-causing mutation (KCNQ1-A341V) associated with high clinical severity. We tested whether the arrhythmic risk was caused directly by A341V or by its presence in the specific ethnic setting of the SA families. | lld:pubmed |
pubmed-article:17984373 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17984373 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17984373 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17984373 | pubmed:language | eng | lld:pubmed |
pubmed-article:17984373 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17984373 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:17984373 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17984373 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17984373 | pubmed:month | Nov | lld:pubmed |
pubmed-article:17984373 | pubmed:issn | 1524-4539 | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:ShimizuWataru... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:SchwartzPeter... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:MossArthur... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:WildeArthur... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:Schulze-BahrE... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:AckermanMicha... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:SwanHeikkiH | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:HorieMinoruM | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:BrinkPaul APA | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:DenjoyIsabell... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:De... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:SpazzoliniCar... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:CrottiLiaL | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:InsoliaRobert... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:Zaklyazminska... | lld:pubmed |
pubmed-article:17984373 | pubmed:author | pubmed-author:CrimiGabriele... | lld:pubmed |
pubmed-article:17984373 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:17984373 | pubmed:day | 20 | lld:pubmed |
pubmed-article:17984373 | pubmed:volume | 116 | lld:pubmed |
pubmed-article:17984373 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17984373 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17984373 | pubmed:pagination | 2366-75 | lld:pubmed |
pubmed-article:17984373 | pubmed:dateRevised | 2008-1-30 | lld:pubmed |
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pubmed-article:17984373 | pubmed:meshHeading | pubmed-meshheading:17984373... | lld:pubmed |
pubmed-article:17984373 | pubmed:meshHeading | pubmed-meshheading:17984373... | lld:pubmed |
pubmed-article:17984373 | pubmed:meshHeading | pubmed-meshheading:17984373... | lld:pubmed |
pubmed-article:17984373 | pubmed:meshHeading | pubmed-meshheading:17984373... | lld:pubmed |
pubmed-article:17984373 | pubmed:meshHeading | pubmed-meshheading:17984373... | lld:pubmed |
pubmed-article:17984373 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17984373 | pubmed:articleTitle | The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification. | lld:pubmed |
pubmed-article:17984373 | pubmed:affiliation | Section of Cardiology, Department of Lung, Blood and Heart, University of Pavia, Pavia, Italy. | lld:pubmed |
pubmed-article:17984373 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17984373 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:17984373 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:17984373 | pubmed:publicationType | Multicenter Study | lld:pubmed |
pubmed-article:17984373 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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