Congenital absence of the vas deferens with hypospadias or without hypospadias: Phenotypic findings and genetic considerations

Congenital absence of the vas deferens (CAVD) is a major cause of obstructive azoospermia. Mutations of CFTR and ADGRG2 cause the majority of CAVD. Despite this, 10%–20% of CAVD patients remain without a clear genetic diagnosis. Herein, the CFTR and ADGRG2 genes were first sequenced using Sanger seq...

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Detalles Bibliográficos
Autores principales: Fang, Jianzheng, Wang, Xiaoyi, Sun, Xueping, Cui, Yugui, Diao, Feiyang, Yang, Xiaoyu
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/PMC9682239/
https://www.ncbi.nlm.nih.gov/pubmed/36437957
http://dx.doi.org/10.3389/fgene.2022.1035468

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682239/
https://www.ncbi.nlm.nih.gov/pubmed/36437957
http://dx.doi.org/10.3389/fgene.2022.1035468

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