Miscues on the "lack of MEF2A mutations" in coronary artery disease.
作者信息
Wang Qing, Rao Shaoqi, Topol Eric J
出版信息
J Clin Invest. 2005 Jun;115(6):1399-400; author reply 1400-1. doi: 10.1172/JCI25475.
Abstract
摘要
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本文引用的文献
1
Lack of MEF2A mutations in coronary artery disease.
J Clin Invest. 2005 Apr;115(4):1016-20. doi: 10.1172/JCI24186.
2
MEF2A sequence variants and coronary artery disease: a change of heart?
J Clin Invest. 2005 Apr;115(4):831-3. doi: 10.1172/JCI24715.
3
Transcription factor MEF2A mutations in patients with coronary artery disease.
Hum Mol Genet. 2004 Dec 15;13(24):3181-8. doi: 10.1093/hmg/ddh329. Epub 2004 Oct 20.
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Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis.
Am J Hum Genet. 2004 Feb;74(2):262-71. doi: 10.1086/381560. Epub 2004 Jan 19.
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