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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Publicado en:Mol Med Rep
Autores principales: Cui, Xiangrong, Wu, Xueqing, Li, Qiang, Jing, Xuan
Formato: Artigo
Lenguaje:Inglês
Publicado: D.A. Spandidos 2020
Materias:
Review
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7533508/
https://ncbi.nlm.nih.gov/pubmed/33000223
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2020.11456
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