Loss‐of‐function mutation in TSGA10 causes acephalic spermatozoa phenotype in human

BACKGROUND: Acephalic spermatozoa is an extremely rare type of teratozoospermia that is associated with male infertility. Several genes have been reported to be relevant to acephalic spermatozoa. Thus, more genetic pathogenesis needs to be explored. METHODS: Whole‐exome sequencing was performed in a...

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Detalles Bibliográficos
Autores principales: Ye, Yuanyuan, Wei, Xiaoli, Sha, Yanwei, Li, Na, Yan, Xiaohong, Cheng, Ling, Qiao, Duanrui, Zhou, Weidong, Wu, Rongfeng, Liu, Qiaobin, Li, Youzhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336754/
https://www.ncbi.nlm.nih.gov/pubmed/32410354
http://dx.doi.org/10.1002/mgg3.1284

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336754/
https://www.ncbi.nlm.nih.gov/pubmed/32410354
http://dx.doi.org/10.1002/mgg3.1284

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