Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans-Reference-Cited by-同舟云学术

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

Published:2021-02 Issue:2 Volume:108 Page:324-336
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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

Funder

Fundamental Research Funds for the Central Universities

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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