Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans

Azoospermia is a significant cause of male infertility, with non-obstructive azoospermia (NOA) being the most severe type of spermatogenic failure. NOA is mostly caused by congenital factors, but our understanding of its genetic causes is very limited. Here, we identified a frameshift variant (c.201...

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Detalles Bibliográficos
Autores principales: Liu, Junyan, Rahim, Fazal, Zhou, Jianteng, Fan, Suixing, Jiang, Hanwei, Yu, Changping, Chen, Jing, Xu, Jianze, Yang, Gang, Shah, Wasim, Zubair, Muhammad, Khan, Asad, Li, Yang, Shah, Basit, Zhao, Daren, Iqbal, Furhan, Jiang, Xiaohua, Guo, Tonghang, Xu, Peng, Xu, Bo, Wu, Limin, Ma, Hui, Zhang, Yuanwei, Zhang, Huan, Shi, Qinghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362269/
https://www.ncbi.nlm.nih.gov/pubmed/37485353
http://dx.doi.org/10.1016/j.isci.2023.107193

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362269/
https://www.ncbi.nlm.nih.gov/pubmed/37485353
http://dx.doi.org/10.1016/j.isci.2023.107193

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