Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility

Acephalic spermatozoa syndrome is a rare type of teratozoospermia that severely impairs the reproductive ability of male patients, and genetic defects have been recognized as the main cause of acephalic spermatozoa syndrome. Spermatogenesis and centriole-associated 1 like (SPATC1L) is indispensable...

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Detalles Bibliográficos
Autores principales: Li, You-Zhu, Li, Na, Liu, Wen-Sheng, Sha, Yan-Wei, Wu, Rong-Feng, Tang, Ya-Ling, Zhu, Xing-Shen, Wei, Xiao-Li, Zhang, Xiao-Ya, Wang, Yi-Feng, Lu, Zhong-Xian, Zhang, Fu-Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8788604/
https://www.ncbi.nlm.nih.gov/pubmed/34213489
http://dx.doi.org/10.4103/aja.aja_56_21

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