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| pubmed-article:19668779 | lifeskim:mentions | umls-concept:C0036572 | lld:lifeskim |
| pubmed-article:19668779 | lifeskim:mentions | umls-concept:C0332307 | lld:lifeskim |
| pubmed-article:19668779 | lifeskim:mentions | umls-concept:C0023976 | lld:lifeskim |
| pubmed-article:19668779 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:19668779 | lifeskim:mentions | umls-concept:C1416572 | lld:lifeskim |
| pubmed-article:19668779 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:19668779 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
| pubmed-article:19668779 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:19668779 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:19668779 | pubmed:dateCreated | 2009-8-11 | lld:pubmed |
| pubmed-article:19668779 | pubmed:abstractText | Long QT syndrome (LQTS) is characterized by corrected QT interval prolongation leading to torsades de pointes and sudden cardiac death. LQTS type 2 (LQTS2) is caused by mutations in the KCNH2 gene, leading to a reduction of the rapidly activating delayed rectifier K+ current and loss of human ether-à-go-go-related gene (hERG) channel function by different mechanisms. Triggers for life-threatening arrhythmias in LQTS2 are often auditory stimuli. | lld:pubmed |
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| pubmed-article:19668779 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19668779 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19668779 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:19668779 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19668779 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:19668779 | pubmed:issn | 1916-7075 | lld:pubmed |
| pubmed-article:19668779 | pubmed:author | pubmed-author:FickerEckhard... | lld:pubmed |
| pubmed-article:19668779 | pubmed:author | pubmed-author:ChahineMohame... | lld:pubmed |
| pubmed-article:19668779 | pubmed:author | pubmed-author:KellerDagmar... | lld:pubmed |
| pubmed-article:19668779 | pubmed:author | pubmed-author:BrinkMarijkeM | lld:pubmed |
| pubmed-article:19668779 | pubmed:author | pubmed-author:OsswaldStefan... | lld:pubmed |
| pubmed-article:19668779 | pubmed:author | pubmed-author:DuboulozFrédé... | lld:pubmed |
| pubmed-article:19668779 | pubmed:author | pubmed-author:ChristéGeorge... | lld:pubmed |
| pubmed-article:19668779 | pubmed:author | pubmed-author:GrenierJulieJ | lld:pubmed |
| pubmed-article:19668779 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19668779 | pubmed:volume | 25 | lld:pubmed |
| pubmed-article:19668779 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19668779 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19668779 | pubmed:pagination | 455-62 | lld:pubmed |
| pubmed-article:19668779 | pubmed:dateRevised | 2010-9-27 | lld:pubmed |
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| pubmed-article:19668779 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19668779 | pubmed:articleTitle | Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures. | lld:pubmed |
| pubmed-article:19668779 | pubmed:affiliation | Cardiology Department, Univesiry Hospital of Basel, Basel, Switzerland. | lld:pubmed |
| pubmed-article:19668779 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19668779 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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