DNA结构变异作为长QT综合征的遗传风险因素。 - Suppr

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超能文献

DNA structural variants as genetic risk factors for the long QT syndrome.

作者信息

Rich Stephen S, Hall Ira M

出版信息

J Am Coll Cardiol. 2011 Jan 4;57(1):48-50. doi: 10.1016/j.jacc.2010.07.040.

DOI:10.1016/j.jacc.2010.07.040

PMID:21185500

Abstract

摘要

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相似文献

DNA structural variants as genetic risk factors for the long QT syndrome.

J Am Coll Cardiol. 2011 Jan 4;57(1):48-50. doi: 10.1016/j.jacc.2010.07.040.

Long QT syndrome - a genetic cardiac channelopathy.

Kardiol Pol. 2010 May;68(5):575-83.

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Trends Genet. 2003 Sep;19(9):470-3. doi: 10.1016/S0168-9525(03)00200-2.

Preventing deaths from long QT syndrome.

CMAJ. 2001 Mar 20;164(6):747-8; author reply 748-9.

[Long QT syndrome--genes, mechanisms and risks. Indication for genetic family screening?].

Ugeskr Laeger. 2006 Jun 26;168(26-32):2537-42.

[Mutational analyses of familial long QT syndrome].

Nihon Rinsho. 1998 Feb;56(2):532-9.

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J Electrocardiol. 2006 Oct;39(4 Suppl):S119-22. doi: 10.1016/j.jelectrocard.2006.06.008. Epub 2006 Aug 21.

Epinephrine QT stress testing in congenital long QT syndrome.

J Electrocardiol. 2006 Oct;39(4 Suppl):S107-13. doi: 10.1016/j.jelectrocard.2006.05.013. Epub 2006 Sep 7.

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Headache. 2007 Jun;47(6):932-3. doi: 10.1111/j.1526-4610.2007.00833.x.

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