A homozygous FANCM frameshift pathogenic variant causes male infertility-Reference-Cited by-同舟云学术

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A homozygous FANCM frameshift pathogenic variant causes male infertility

Published:2019-01 Issue:1 Volume:21 Page:62-70
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Yin Hao,Ma Hui,Hussain Sajjad,Zhang Huan,Xie Xuefeng,Jiang Long,Jiang Xiaohua,Iqbal Furhan,Bukhari Ihtisham,Jiang Hanwei,Ali Asim,Zhong Liangwen,Li Tao,Fan Suixing,Zhang Beibei,Gao Jianing,Li Yang,Nazish Jabeen,Khan Teka,Khan Manan,Zubair Muhammad,Hao Qiaomei,Fang Hui,Huang Jun,Huleihel Mahmoud,Sha Jiahao,Pandita Tej K.,Zhang Yuanwei,Shi Qinghua

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

https://www.nature.com/articles/s41436-018-0015-7.pdf

Reference35 articles.

Cited by 81 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A novel homozygous splicing mutation in AK7 causes multiple morphological abnormalities of sperm flagella in patients from consanguineous Pakistani families;Asian Journal of Andrology;2024-09-10

2. Fance deficiency impaired DNA damage repair of prospermatogonia and altered the repair dynamics of spermatocytes;Reproductive Biology and Endocrinology;2024-08-29

3. Deficiency in a special dynein DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and mice;2024-08-27

4. Deficiency in a special dynein DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and mice;2024-08-27

5. Sperm from infertile, oligozoospermic men have elevated mutation rates;2024-08-22

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