Cargando…
A novel homozygous loss-of-function mutation in RAD51AP2 induces male infertility with nonobstructive azoospermia
Autores principales: | Liu, Liu, Tang, Shu-Yan, Zhang, Feng, Jiang, Feng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226490/ https://www.ncbi.nlm.nih.gov/pubmed/36153927 http://dx.doi.org/10.4103/aja202272 |
Ejemplares similares
-
Clinical management of infertile men with nonobstructive azoospermia
por: Esteves, Sandro C
Publicado: (2015) -
MBOAT1 homozygous missense variant causes nonobstructive azoospermia
por: Wan, Yang-Yang, et al.
Publicado: (2021) -
Altered Gene Expression in the Testis of Infertile Patients with Nonobstructive Azoospermia
por: Wang, Zhiqiang, et al.
Publicado: (2021) -
ESX1 gene as a potential candidate responsible for male infertility in nonobstructive azoospermia
por: Malcher, Agnieszka, et al.
Publicado: (2023) -
Infertility network and hub genes for nonobstructive azoospermia utilizing integrative analysis
por: Han, Baoquan, et al.
Publicado: (2021)