Fetal Congenital Heart Disease Caused by Compound Heterozygous Mutations in the DNAH9 Gene: A Case Report

Fetal Congenital Heart Disease Caused by Compound Heterozygous Mutations in the DNAH9 Gene: A Case Report

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 and effective prenatal diagnosis is very important for the preventio...

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Bibliographic Details
Main Authors: Tao Zhang, Hua Yuan, Hongdan Zhu, Yuyi Ying, Jinlong Ding, Haigang Ding, Xiaoliang Shi, Yao He, Haitao Pan, Yongxing Zhong
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-01-01
Series:Frontiers in Genetics
Subjects:
congenital heart disease
DNAH9 gene
copy number variation sequencing
whole exome sequencing
3D structure
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.771756/full

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https://www.frontiersin.org/articles/10.3389/fgene.2021.771756/full

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