pubmed-article:10525521 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10525521 | lifeskim:mentions | umls-concept:C1420562 | lld:lifeskim |
pubmed-article:10525521 | lifeskim:mentions | umls-concept:C0949658 | lld:lifeskim |
pubmed-article:10525521 | lifeskim:mentions | umls-concept:C0149721 | lld:lifeskim |
pubmed-article:10525521 | lifeskim:mentions | umls-concept:C0522086 | lld:lifeskim |
pubmed-article:10525521 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:10525521 | lifeskim:mentions | umls-concept:C0678227 | lld:lifeskim |
pubmed-article:10525521 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:10525521 | pubmed:dateCreated | 1999-12-23 | lld:pubmed |
pubmed-article:10525521 | pubmed:abstractText | To screen for a mutation of the cardiac troponin T gene in two families where there had been sudden deaths without an increase in left ventricular mass but with myocardial disarray suggesting hypertrophic cardiomyopathy. | lld:pubmed |
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pubmed-article:10525521 | pubmed:language | eng | lld:pubmed |
pubmed-article:10525521 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10525521 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:10525521 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10525521 | pubmed:month | Nov | lld:pubmed |
pubmed-article:10525521 | pubmed:issn | 1468-201X | lld:pubmed |
pubmed-article:10525521 | pubmed:author | pubmed-author:DaviesM JMJ | lld:pubmed |
pubmed-article:10525521 | pubmed:author | pubmed-author:ElliottP MPM | lld:pubmed |
pubmed-article:10525521 | pubmed:author | pubmed-author:McKennaW JWJ | lld:pubmed |
pubmed-article:10525521 | pubmed:author | pubmed-author:DavisonFF | lld:pubmed |
pubmed-article:10525521 | pubmed:author | pubmed-author:BaboonianCC | lld:pubmed |
pubmed-article:10525521 | pubmed:author | pubmed-author:VarnavaAA | lld:pubmed |
pubmed-article:10525521 | pubmed:author | pubmed-author:de CruzLL | lld:pubmed |
pubmed-article:10525521 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:10525521 | pubmed:volume | 82 | lld:pubmed |
pubmed-article:10525521 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10525521 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10525521 | pubmed:pagination | 621-4 | lld:pubmed |
pubmed-article:10525521 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:10525521 | pubmed:year | 1999 | lld:pubmed |
pubmed-article:10525521 | pubmed:articleTitle | A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy. | lld:pubmed |
pubmed-article:10525521 | pubmed:affiliation | Department of Cardiological Sciences, St George's Hospital Medical School, Cranmer Terrace, London SW17 ORE, UK. | lld:pubmed |
pubmed-article:10525521 | pubmed:publicationType | Journal Article | lld:pubmed |
entrez-gene:7139 | entrezgene:pubmed | pubmed-article:10525521 | lld:entrezgene |
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