Novel mutations of PMFBP1 in a man with acephalic spermatozoa defects

BACKGROUND: Acephalic spermatozoa (AS) is a serious but rare reproductive genetic disorder that causes infertility in men. To date, only a few genes associated with AS defects have been identified, including the polyamine modulated factor 1 binding protein 1 (PMFBP1) gene. Consistent with this, PMFB...

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Detalles Bibliográficos
Autores principales: Nie, Hua, Tang, Yunge, Zhang, Xiaoyu, Tan, Yuqiu, Qin, Weibing
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/PMC9482405/
https://www.ncbi.nlm.nih.gov/pubmed/35860846
http://dx.doi.org/10.1002/mgg3.2020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482405/
https://www.ncbi.nlm.nih.gov/pubmed/35860846
http://dx.doi.org/10.1002/mgg3.2020

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