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| pubmed-article:11897440 | lifeskim:mentions | umls-concept:C0007193 | lld:lifeskim |
| pubmed-article:11897440 | lifeskim:mentions | umls-concept:C0004245 | lld:lifeskim |
| pubmed-article:11897440 | lifeskim:mentions | umls-concept:C0443147 | lld:lifeskim |
| pubmed-article:11897440 | lifeskim:mentions | umls-concept:C1416877 | lld:lifeskim |
| pubmed-article:11897440 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:11897440 | pubmed:dateCreated | 2002-3-18 | lld:pubmed |
| pubmed-article:11897440 | pubmed:abstractText | We investigated the prevalence of lamin A/C (LMNA) gene defects in familial and sporadic dilated cardiomyopathies (DCM) associated with atrioventricular block (AVB) or increased serum creatine-phosphokinase (sCPK), and the corresponding changes in myocardial and protein expression. | lld:pubmed |
| pubmed-article:11897440 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:11897440 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:11897440 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11897440 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:11897440 | pubmed:issn | 0735-1097 | lld:pubmed |
| pubmed-article:11897440 | pubmed:author | pubmed-author:TavazziLuigiL | lld:pubmed |
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| pubmed-article:11897440 | pubmed:author | pubmed-author:NegriAndreaA | lld:pubmed |
| pubmed-article:11897440 | pubmed:author | pubmed-author:DiegoliMartaM | lld:pubmed |
| pubmed-article:11897440 | pubmed:author | pubmed-author:ScelsiLauraL | lld:pubmed |
| pubmed-article:11897440 | pubmed:author | pubmed-author:BaldiniElisaE | lld:pubmed |
| pubmed-article:11897440 | pubmed:author | pubmed-author:GavazziAntone... | lld:pubmed |
| pubmed-article:11897440 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11897440 | pubmed:day | 20 | lld:pubmed |
| pubmed-article:11897440 | pubmed:volume | 39 | lld:pubmed |
| pubmed-article:11897440 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11897440 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11897440 | pubmed:pagination | 981-90 | lld:pubmed |
| pubmed-article:11897440 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:11897440 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:11897440 | pubmed:articleTitle | Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease. | lld:pubmed |
| pubmed-article:11897440 | pubmed:affiliation | Molecular Diagnostic Division, IRCCS Policlinico San Matteo, Pavia, Italy. e.arbustini@smatteo.pv.it | lld:pubmed |
| pubmed-article:11897440 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11897440 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:11897440 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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