Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia

Background: Severe spermatogenic failure (SPGF) represents one of the most relevant causes of male infertility. This pathological condition can lead to extreme abnormalities in the seminal sperm count, such as severe oligozoospermia (SO) or non-obstructive azoospermia (NOA). Most cases of SPGF have...

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Detalles Bibliográficos
Autores principales: Guzmán-Jiménez, Andrea, González-Muñoz, Sara, Cerván-Martín, Miriam, Rivera-Egea, Rocío, Garrido, Nicolás, Luján, Saturnino, Santos-Ribeiro, Samuel, Castilla, José A., Gonzalvo, M. Carmen, Clavero, Ana, Vicente, F. Javier, Maldonado, Vicente, Villegas-Salmerón, Javier, Burgos, Miguel, Jiménez, Rafael, Pinto, Maria Graça, Pereira, Isabel, Nunes, Joaquim, Sánchez-Curbelo, Josvany, López-Rodrigo, Olga, Pereira-Caetano, Iris, Marques, Patricia Isabel, Carvalho, Filipa, Barros, Alberto, Bassas, Lluís, Seixas, Susana, Gonçalves, João, Lopes, Alexandra M., Larriba, Sara, Palomino-Morales, Rogelio J., Carmona, F. David, Bossini-Castillo, Lara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797780/
https://www.ncbi.nlm.nih.gov/pubmed/36589743
http://dx.doi.org/10.3389/fcell.2022.1089782

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797780/
https://www.ncbi.nlm.nih.gov/pubmed/36589743
http://dx.doi.org/10.3389/fcell.2022.1089782

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