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| pubmed-article:20031595 | lifeskim:mentions | umls-concept:C0330390 | lld:lifeskim |
| pubmed-article:20031595 | lifeskim:mentions | umls-concept:C0018787 | lld:lifeskim |
| pubmed-article:20031595 | lifeskim:mentions | umls-concept:C1623258 | lld:lifeskim |
| pubmed-article:20031595 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:20031595 | lifeskim:mentions | umls-concept:C0037492 | lld:lifeskim |
| pubmed-article:20031595 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
| pubmed-article:20031595 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:20031595 | lifeskim:mentions | umls-concept:C1711351 | lld:lifeskim |
| pubmed-article:20031595 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:20031595 | pubmed:dateCreated | 2009-12-24 | lld:pubmed |
| pubmed-article:20031595 | pubmed:abstractText | Brugada syndrome, characterized by ST-segment elevation in the right precordial ECG leads and the development of life-threatening ventricular arrhythmias, has been associated with mutations in 6 different genes. We identify and characterize a mutation in a new gene. | lld:pubmed |
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| pubmed-article:20031595 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:20031595 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:20031595 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20031595 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:20031595 | pubmed:issn | 1942-3268 | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:AntzelevitchC... | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:PollevickGuid... | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:GuerchicoffAl... | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:CordeiroJonat... | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:BRUYY | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:VarroAndrasA | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:KoopmannTamar... | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:SpringerMicha... | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:BurashnikovEl... | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:Barajas-Marti... | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:PfeifferRyanR | lld:pubmed |
| pubmed-article:20031595 | pubmed:author | pubmed-author:WuYueshengY | lld:pubmed |
| pubmed-article:20031595 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20031595 | pubmed:volume | 2 | lld:pubmed |
| pubmed-article:20031595 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20031595 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20031595 | pubmed:pagination | 270-8 | lld:pubmed |
| pubmed-article:20031595 | pubmed:dateRevised | 2011-10-20 | lld:pubmed |
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| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:meshHeading | pubmed-meshheading:20031595... | lld:pubmed |
| pubmed-article:20031595 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:20031595 | pubmed:articleTitle | A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype. | lld:pubmed |
| pubmed-article:20031595 | pubmed:affiliation | Masonic Medical Research Laboratory, Utica, NY, USA. | lld:pubmed |
| pubmed-article:20031595 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20031595 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:20031595 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:20031595 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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