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Atrial Septal Defect(ASD)associated long non-coding RNA STX18-AS1 maintains time-course of in vitro cardiomyocyte differentiation
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作者 Yingjuan Liu Mun-kit Choy +3 位作者 Sabu Abraham Gennadiy Tenin graeme c.black Bernard D.Keavney 《Genes & Diseases》 SCIE CSCD 2023年第4期1150-1153,共4页
Congenital heart disease(CHD)is the commonest birth defect,affecting approximately 9.4/1000 live births.^(1)Atrial Septal Defect(ASD)is one of the commonest CHD clinical phenotypes,which frequently requires treatment ... Congenital heart disease(CHD)is the commonest birth defect,affecting approximately 9.4/1000 live births.^(1)Atrial Septal Defect(ASD)is one of the commonest CHD clinical phenotypes,which frequently requires treatment either in childhood or adulthood,and can lead to severe complications such as right heart failure and cardiac arrhythmia.Previous genome-wide association studies(GWAS)have identified a region of chromosome 4p16(Ch4p16)associated with the risk of ASD. 展开更多
关键词 clinical MAINTAIN CARDIAC
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