Načítá se...

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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Mol Med Rep
Hlavní autoři: Cui, Xiangrong, Wu, Xueqing, Li, Qiang, Jing, Xuan
Médium: Artigo
Jazyk:Inglês
Vydáno: D.A. Spandidos 2020
Témata:
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!