期刊文献+

先天性心脏病患者远期并发心律失常的分子遗传学机制

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摘要 先天性心脏病(congenital heart disease,CHD)是一种最常见的出生缺陷,为自然流产和死胎最常见的原因之一。最近研究提示,在心脏发育中,NKx2.5,SCN5A等基因的异常,不但会导致人类CHD的发生,而且可能会影响成年后心脏的正常功能。CHD患者远期并发的心脏疾患可能与这些基因的异常有关。
出处 《心脏杂志》 CAS 2010年第2期282-284,288,共4页 Chinese Heart Journal
基金 陕西省科技攻关项目资助(2007K13-03)
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参考文献9

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