Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans
C14orf39/SIX6OS1基因的纯合突变会导致人类非梗阻性无精子症和卵巢早衰。
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2022.06.006
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