Common genetic variation in KATNAL1 non‐coding regions is involved in the susceptibility to severe phenotypes of male infertility

BACKGROUND: Previous studies in animal models evidenced that genetic mutations of KATNAL1, resulting in dysfunction of its encoded protein, lead to male infertility through disruption of microtubule remodelling and premature germ cell exfoliation. Subsequent studies in humans also suggested a possib...

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Detalles Bibliográficos
Autores principales: Cerván‐Martín, Miriam, Bossini‐Castillo, Lara, Guzmán‐Jiménez, Andrea, Rivera‐Egea, Rocío, Garrido, Nicolás, Lujan, Saturnino, Romeu, Gema, Santos‐Ribeiro, Samuel, Castilla, José Antonio, Gonzalvo, María del Carmen, Clavero, Ana, Maldonado, Vicente, Vicente, Francisco Javier, Burgos, Miguel, Jiménez, Rafael, González‐Muñoz, Sara, Sánchez‐Curbelo, Josvany, López‐Rodrigo, Olga, Pereira‐Caetano, Iris, Marques, Patricia Isabel, Carvalho, Filipa, Barros, Alberto, Bassas, Lluís, Seixas, Susana, Gonçalves, João, Larriba, Sara, Lopes, Alexandra Manuel, Palomino‐Morales, Rogelio Jesús, Carmona, Francisco David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546047/
https://www.ncbi.nlm.nih.gov/pubmed/35752927
http://dx.doi.org/10.1111/andr.13221

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546047/
https://www.ncbi.nlm.nih.gov/pubmed/35752927
http://dx.doi.org/10.1111/andr.13221

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