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A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death.
Clin Chim Acta. 2011 Jan 14;412(1-2):170-5. doi: 10.1016/j.cca.2010.09.035. Epub 2010 Oct 4.
Clin Chim Acta. 2011.
PMID: 20932824
Free PMC article.
Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population.
Wang AZ, Li L, Zhang B, Shen GQ, Wang QK.
Wang AZ, et al.
Ann Hum Genet. 2011 Jul;75(4):475-82. doi: 10.1111/j.1469-1809.2011.00646.x. Epub 2011 Apr 4.
Ann Hum Genet. 2011.
PMID: 21463265
Free PMC article.
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