Detection of Novel Pathogenic Variants in Two Families with Recurrent Fetal Congenital Heart Defects

BACKGROUND: Congenital heart disease (CHD) is the most common birth defect with strong genetic heterogeneity. To date, about 400 genes have been linked to CHD, including cell signaling molecules, transcription factors, and structural proteins that are important for heart development. Genetic analysi...

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Detalles Bibliográficos
Autores principales: Cai, Rongqin, Tan, Ya, Wang, Mingming, Yu, Huijun, Wang, Jing, Ren, Zhuo, Dong, Zhe, He, Yiwen, Li, Zhi, Lin, Li, Gu, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008912/
https://www.ncbi.nlm.nih.gov/pubmed/36923242
http://dx.doi.org/10.2147/PGPM.S394120

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008912/
https://www.ncbi.nlm.nih.gov/pubmed/36923242
http://dx.doi.org/10.2147/PGPM.S394120

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