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| pubmed-article:16239976 | lifeskim:mentions | umls-concept:C1142166 | lld:lifeskim |
| pubmed-article:16239976 | lifeskim:mentions | umls-concept:C1419864 | lld:lifeskim |
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| pubmed-article:16239976 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:16239976 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:16239976 | pubmed:dateCreated | 2005-10-21 | lld:pubmed |
| pubmed-article:16239976 | pubmed:abstractText | Brugada syndrome (BS) is an electrical cardiac disorder with a right bundle branch block and ST segment elevation in leads V1 to V3 on surface electrocardiograms (ECGs), and is a syndrome that may lead to sudden cardiac death. | lld:pubmed |
| pubmed-article:16239976 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:16239976 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16239976 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:16239976 | pubmed:issn | 0828-282X | lld:pubmed |
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| pubmed-article:16239976 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16239976 | pubmed:volume | 21 | lld:pubmed |
| pubmed-article:16239976 | pubmed:owner | NLM | lld:pubmed |
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| pubmed-article:16239976 | pubmed:dateRevised | 2011-7-22 | lld:pubmed |
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| pubmed-article:16239976 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:16239976 | pubmed:articleTitle | A novel nonsense mutation in the SCN5A gene leads to Brugada syndrome and a silent gene mutation carrier state. | lld:pubmed |
| pubmed-article:16239976 | pubmed:affiliation | Institut national de la santé et de la recherche médicale U582, Institut Fédératif de Recherche No 14, Pitié-Salpêtrière Hospital, Paris, France. | lld:pubmed |
| pubmed-article:16239976 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16239976 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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