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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2006 | 2 |
2008 | 1 |
2024 | 0 |
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Page 1
Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers.
Scand J Clin Lab Invest. 2008;68(5):362-8. doi: 10.1080/00365510701765643.
Scand J Clin Lab Invest. 2008.
PMID: 18752142
MinK gene polymorphism in the pathogenesis of lone atrial fibrillation.
Prystupa A, Dzida G, Myśliński W, Małaj G, Lorenc T.
Prystupa A, et al.
Kardiol Pol. 2006 Nov;64(11):1205-11; discussion 1212-3.
Kardiol Pol. 2006.
PMID: 17165161
English, Polish.
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Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation.
Fatini C, Sticchi E, Genuardi M, Sofi F, Gensini F, Gori AM, Lenti M, Michelucci A, Abbate R, Gensini GF.
Fatini C, et al.
Eur Heart J. 2006 Jul;27(14):1712-8. doi: 10.1093/eurheartj/ehl087. Epub 2006 Jun 7.
Eur Heart J. 2006.
PMID: 16760206
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