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| pubmed-article:12106942 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:12106942 | pubmed:dateCreated | 2002-7-10 | lld:pubmed |
| pubmed-article:12106942 | pubmed:abstractText | We sought to establish the role of genetic screening for ryanodine receptor type 2 (RyR2) gene mutations in families with effort-induced polymorphic ventricular arrhythmia (PVA), syncope and juvenile sudden death. | lld:pubmed |
| pubmed-article:12106942 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:12106942 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:12106942 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12106942 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:12106942 | pubmed:issn | 0735-1097 | lld:pubmed |
| pubmed-article:12106942 | pubmed:author | pubmed-author:ThieneGaetano... | lld:pubmed |
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| pubmed-article:12106942 | pubmed:volume | 40 | lld:pubmed |
| pubmed-article:12106942 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12106942 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12106942 | pubmed:pagination | 341-9 | lld:pubmed |
| pubmed-article:12106942 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:12106942 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12106942 | pubmed:articleTitle | Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. | lld:pubmed |
| pubmed-article:12106942 | pubmed:affiliation | Department of Cardiology, University of Padua Medical School, Via A. Gabelli, 86-35121 Padua, Italy. | lld:pubmed |
| pubmed-article:12106942 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12106942 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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