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Nkx2.5基因与先天性心脏病 被引量:9

Gene Nkx2.5 and congenital heart disease
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摘要 先天性心脏病(CHD)是人类出生缺陷中最常见的畸形,也是婴幼儿非感染性疾病中最主要的死亡原因。大量研究表明Nkx2.5是重要的转录因子,在心脏发育过程中起很重要的作用,该基因的突变将影响心脏发育导致先心病。本文就Nkx2.5基因与先心病的关系与最新进展予以综述。 Common birth defect, also is the leading cause of death in non - infectious diseases of infants. Numerous studies show that Nkx2. 5 is important transcription factor that plays an important role during cardiac development, the mutation will affect the devel- opment of the heart lead to congenital heart disease. In the present review, the relationship and the current progress of Nkx2. 5 and congenital heart disease were summarized.
作者 蔡花 付四清
出处 《中国优生与遗传杂志》 2014年第4期1-3,共3页 Chinese Journal of Birth Health & Heredity
关键词 先天性心脏病 Nkx2 5 基因突变 Congenital heart disease Nkx2. 5 Gene mutation
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参考文献22

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