| pubmed-article:9753711 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9753711 | lifeskim:mentions | umls-concept:C1257890 | lld:lifeskim |
| pubmed-article:9753711 | lifeskim:mentions | umls-concept:C0035168 | lld:lifeskim |
| pubmed-article:9753711 | lifeskim:mentions | umls-concept:C0449259 | lld:lifeskim |
| pubmed-article:9753711 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
| pubmed-article:9753711 | lifeskim:mentions | umls-concept:C0017431 | lld:lifeskim |
| pubmed-article:9753711 | lifeskim:mentions | umls-concept:C0034975 | lld:lifeskim |
| pubmed-article:9753711 | lifeskim:mentions | umls-concept:C1512888 | lld:lifeskim |
| pubmed-article:9753711 | pubmed:issue | 14 | lld:pubmed |
| pubmed-article:9753711 | pubmed:dateCreated | 1998-10-6 | lld:pubmed |
| pubmed-article:9753711 | pubmed:abstractText | The congenital long-QT syndrome, caused by mutations in cardiac potassium-channel genes (KVLQT1 at the LQT1 locus and HERG at the LQT2 locus) and the sodium-channel gene (SCN5A at the LQT3 locus), has distinct repolarization patterns on electrocardiography, but it is not known whether the genotype influences the clinical course of the disease. | lld:pubmed |
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| pubmed-article:9753711 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9753711 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9753711 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:9753711 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9753711 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:9753711 | pubmed:issn | 0028-4793 | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:RobinsonJ LJL | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:SchwartzP JPJ | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:MossA JAJ | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:HallW JWJ | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:KeatingM TMT | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:VincentG MGM | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:LocatiE HEH | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:TowbinJ AJA | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:PrioriS GSG | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:LehmannM HMH | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:BenhorinJJ | lld:pubmed |
| pubmed-article:9753711 | pubmed:author | pubmed-author:ZarebaWW | lld:pubmed |
| pubmed-article:9753711 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9753711 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:9753711 | pubmed:volume | 339 | lld:pubmed |
| pubmed-article:9753711 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9753711 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9753711 | pubmed:pagination | 960-5 | lld:pubmed |
| pubmed-article:9753711 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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| pubmed-article:9753711 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9753711 | pubmed:articleTitle | Influence of genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group. | lld:pubmed |
| pubmed-article:9753711 | pubmed:affiliation | Department of Medicine, University of Rochester School of Medicine and Dentistry, NY, USA. | lld:pubmed |
| pubmed-article:9753711 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9753711 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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