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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Detalles Bibliográficos
Autores principales: Zhang, Tao, Yuan, Hua, Zhu, Hongdan, Ying, Yuyi, Ding, Jinlong, Ding, Haigang, Shi, Xiaoliang, He, Yao, Pan, Haitao, Zhong, Yongxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804278/
https://www.ncbi.nlm.nih.gov/pubmed/35116053
http://dx.doi.org/10.3389/fgene.2021.771756

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804278/
https://www.ncbi.nlm.nih.gov/pubmed/35116053
http://dx.doi.org/10.3389/fgene.2021.771756

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