Identification of zona pellucida defects revealed a novel loss-of-function mutation in ZP2 in humans and rats

INTRODUCTION: Human zona pellucida (ZP) plays an important role in reproductive process. Several rare mutations in the encoding genes (ZP1, ZP2, and ZP3) have been demonstrated to cause women infertility. Mutations in ZP2 have been reported to cause ZP defects or empty follicle syndrome. We aimed to...

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Detalles Bibliográficos
Autores principales: Zeng, Jun, Sun, Ying, Zhang, Jing, Wu, Xiaozhu, Wang, Yan, Quan, Ruping, Song, Wanjuan, Guo, Dan, Wang, Shengran, Chen, Jianlin, Xiao, Hongmei, Huang, Hua-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244809/
https://www.ncbi.nlm.nih.gov/pubmed/37293489
http://dx.doi.org/10.3389/fendo.2023.1169378

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244809/
https://www.ncbi.nlm.nih.gov/pubmed/37293489
http://dx.doi.org/10.3389/fendo.2023.1169378

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