Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling

Congenital bilateral absence of the vas deferens (CBAVD) is predominantly caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. CBAVD accounts for 2–6% of male infertility cases and up to 25% of cases of obstructive azoospermia. With the use of pre-implantation...

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Detalles Bibliográficos
Autores principales: Cui, Xiangrong, Wu, Xueqing, Li, Qiang, Jing, Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533508/
https://www.ncbi.nlm.nih.gov/pubmed/33000223
http://dx.doi.org/10.3892/mmr.2020.11456

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533508/
https://www.ncbi.nlm.nih.gov/pubmed/33000223
http://dx.doi.org/10.3892/mmr.2020.11456

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