TY  - JOUR
AU  - Cerván-Martín, Miriam
AU  - Bossini-Castillo, Lara
AU  - Guzmán-Jiménez, Andrea
AU  - Rivera-Egea, Rocío
AU  - Garrido, Nicolás
AU  - Lujan, Saturnino
AU  - Romeu, Gema
AU  - Santos-Ribeiro, Samuel
AU  - IVIRMA Group
AU  - Lisbon Clinical Group
AU  - Castilla, José Antonio
AU  - Gonzalvo, María Del Carmen
AU  - Clavero, Ana
AU  - Maldonado, Vicente
AU  - Vicente, Francisco Javier
AU  - Burgos, Miguel
AU  - Jiménez, Rafael
AU  - González-Muñoz, Sara
AU  - Sánchez-Curbelo, Josvany
AU  - López-Rodrigo, Olga
AU  - Pereira-Caetano, Iris
AU  - Marques, Patricia Isabel
AU  - Carvalho, Filipa
AU  - Barros, Alberto
AU  - Bassas, Lluís
AU  - Seixas, Susana
AU  - Gonçalves, João
AU  - Larriba, Sara
AU  - Lopes, Alexandra Manuel
AU  - Palomino-Morales, Rogelio Jesús
AU  - Carmona, Francisco David
PY  - 2022
DO  - 10.1111/andr.13221
UR  - http://hdl.handle.net/10668/19906
T2  - Andrology
AB  - 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...
LA  - en
KW  - KATNAL1
KW  - SNP
KW  - male infertility
KW  - spermatogenesis
KW  - splicing
KW  - Animals
KW  - Humans
KW  - Male
KW  - Azoospermia
KW  - Infertility, Male
KW  - Katanin
KW  - Oligospermia
KW  - Phenotype
KW  - Polymorphism, Single Nucleotide
KW  - Protein Isoforms
KW  - Semen
KW  - Spermatogenesis
TI  - Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.
TY  - research article
VL  - 10
ER  -