Preprint
Familial primary ovarian insufficiency associated with an SYCE1 point mutation: defective meiosis elucidated in humanized mice
Fecha
2020Registro en:
Hernández López, D, Geisinger Wschebor, A, Trovero Martínez, M, [y otro]. "Familial primary ovarian insufficiency associated with an SYCE1 point mutation: defective meiosis elucidated in humanized mice" [Preprint]. Publicado en: Molecular Human Reproduction, 2020, 26(7): 485–497, doi: 10.1093/molehr/gaaa032
Autor
Hernández López, Diego
Geisinger Wschebor, Adriana
Trovero Martínez, María Fernanda
Santiñaque, Federico
Brauer, Mónica
Folle Ungo, Gustavo A.
Benavente, Ricardo
Rodríguez-Casuriaga, Rosana