| pubmed-article:15828882 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15828882 | lifeskim:mentions | umls-concept:C0004238 | lld:lifeskim |
| pubmed-article:15828882 | lifeskim:mentions | umls-concept:C2348199 | lld:lifeskim |
| pubmed-article:15828882 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:15828882 | lifeskim:mentions | umls-concept:C1416572 | lld:lifeskim |
| pubmed-article:15828882 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
| pubmed-article:15828882 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:15828882 | pubmed:dateCreated | 2005-4-14 | lld:pubmed |
| pubmed-article:15828882 | pubmed:abstractText | The short QT syndrome is a newly described clinical entity characterized by the presence of a short QT interval associated with cardiac tachyarrhythmias including sudden cardiac death at a young age in otherwise healthy individuals. A genetic basis has been identified linking the disease to mutations in KCNH2 in the familial forms and a mutation in KCNQ1 in a sporadic form of the disease. | lld:pubmed |
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| pubmed-article:15828882 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15828882 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15828882 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:15828882 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15828882 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:15828882 | pubmed:issn | 1045-3873 | lld:pubmed |
| pubmed-article:15828882 | pubmed:author | pubmed-author:HeckD VDV | lld:pubmed |
| pubmed-article:15828882 | pubmed:author | pubmed-author:BrugadaRamonR | lld:pubmed |
| pubmed-article:15828882 | pubmed:author | pubmed-author:BjerregaardPr... | lld:pubmed |
| pubmed-article:15828882 | pubmed:author | pubmed-author:GussakIhorI | lld:pubmed |
| pubmed-article:15828882 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15828882 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:15828882 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15828882 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15828882 | pubmed:pagination | 394-6 | lld:pubmed |
| pubmed-article:15828882 | pubmed:dateRevised | 2008-10-28 | lld:pubmed |
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| pubmed-article:15828882 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15828882 | pubmed:articleTitle | Short QT syndrome and atrial fibrillation caused by mutation in KCNH2. | lld:pubmed |
| pubmed-article:15828882 | pubmed:affiliation | Molecular Genetics, Masonic Medical Research Laboratory, Utica, New York, USA. | lld:pubmed |
| pubmed-article:15828882 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15828882 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:15828882 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:15828882 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:15828882 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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