Novel mutations in the lamin A/C gene in heart transplant recipients with end stage dilated cardiomyopathy.
作者信息
Kärkkäinen S, Reissell E, Heliö T, Kaartinen M, Tuomainen P, Toivonen L, Kuusisto J, Kupari M, Nieminen M S, Laakso M, Peuhkurinen K
出版信息
Heart. 2006 Apr;92(4):524-6. doi: 10.1136/hrt.2004.056721.
Abstract
摘要
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本文引用的文献
1
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Eur Heart J. 2004 May;25(10):885-93. doi: 10.1016/j.ehj.2004.01.020.
2
Loss of lamin A/C expression revealed by immuno-electron microscopy in dilated cardiomyopathy with atrioventricular block caused by LMNA gene defects.
Virchows Arch. 2003 Nov;443(5):664-71. doi: 10.1007/s00428-003-0865-4. Epub 2003 Jul 26.
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Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.
J Am Coll Cardiol. 2003 Mar 5;41(5):771-80. doi: 10.1016/s0735-1097(02)02954-6.
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Molecular mechanisms of inherited cardiomyopathies.
Physiol Rev. 2002 Oct;82(4):945-80. doi: 10.1152/physrev.00012.2002.
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Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease.
J Am Coll Cardiol. 2002 Mar 20;39(6):981-90. doi: 10.1016/s0735-1097(02)01724-2.
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Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
N Engl J Med. 1999 Dec 2;341(23):1715-24. doi: 10.1056/NEJM199912023412302.
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