Fetal Congenital Heart Disease Caused by Compound Heterozygous Mutations in the DNAH9 Gene: A Case Report
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DOI: 10.3389/fgene.2021.771756
Abstract: Background: Fetal congenital heart disease (CHD) is the most common congenital defect, with an incidence of 0.6–0.8%, accounting for 30–50% of infant congenital disease deaths. The pathogenesis of CHD is still unclear, so an active… read more here.
Keywords: chd; dnah9 gene; disease; fetal congenital ... See more keywords