Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.

Fan, Suixing; Jiao, Yuying; Khan, Ranjha; Jiang, Xiaohua; Javed, Abdul Rafay; Ali, Asim; Zhang, Huan; Zhou, Jianteng; Naeem, Muhammad; Murtaza, Ghulam; Li, Yang; Yang, Gang; Zaman, Qumar; Zubair, Muhammad; Guan, Haiyang; Zhang, Xingxia; Ma, Hui; Jiang, Hanwei; Ali, Haider; Dil, Sobia; Shah, Wasim; Ahmad, Niaz; Zhang, Yuanwei; Shi, Qinghua

Fan, Suixing; Jiao, Yuying; Khan, Ranjha; Jiang, Xiaohua; Javed, Abdul Rafay; Ali, Asim; Zhang, Huan; Zhou, Jianteng; Naeem, Muhammad; Murtaza, Ghulam; Li, Yang; Yang, Gang; Zaman, Qumar; Zubair, Muhammad; Guan, Haiyang; Zhang, Xingxia; Ma, Hui; Jiang, Hanwei; Ali, Haider; Dil, Sobia; Shah, Wasim; Ahmad, Niaz; Zhang, Yuanwei; Shi, Qinghua.

Am J Hum Genet ; 109(7): 1343, 2022 Jul 07.

Article en En | MEDLINE | ID: mdl-35803236

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300872
https://dx.doi.org/10.1016/j.ajhg.2022.06.006

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Am J Hum Genet Año: 2022 Tipo del documento: Article

Texto completo

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300872
https://dx.doi.org/10.1016/j.ajhg.2022.06.006

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Am J Hum Genet Año: 2022 Tipo del documento: Article