Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility
Ma, Ao, Zeb, Aurang, Ali, Imtiaz, Zhao, Daren, Khan, Asad, Zhang, Beibei, Zhou, Jianteng, Khan, Ranjha, Zhang, Huan, Zhang, Yuanwei, Khan, Ihsan, Shah, Wasim, Ali, Haider, Javed, Abdul Rafay, Ma, Hui, Shi, Qinghua
Published in Frontiers in cell and developmental biology (31.01.2022)
Published in Frontiers in cell and developmental biology (31.01.2022)
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Journal Article
Computationally predicted pathogenic USP9X mutation identified in infertile men does not affect spermatogenesis in mice
Liu, Wei, Wang, Yue-Wen, Zhang, Huan, Xie, Xue-Feng, Ma, Ao, Zaman, Qumar, Javed, Abdul Rafay, Abbas, Tanveer, Shah, Wasim, Ahmad, Riaz, Zhao, Da-Ren, Ma, Hui, Zubair, Muhammad, Khan, Ranjha, Shi, Qing-Hua
Published in Dōngwùxué yánjiū (18.03.2022)
Published in Dōngwùxué yánjiū (18.03.2022)
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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
Published in American journal of human genetics (04.02.2021)
Published in American journal of human genetics (04.02.2021)
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Journal Article
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
Published in American journal of human genetics (07.07.2022)
Published in American journal of human genetics (07.07.2022)
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Journal Article