当前位置:
X-MOL 学术
›
J. Genet. Genomics
›
论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia.
Journal of Genetics and Genomics ( IF 5.9 ) Pub Date : 2018-12-06 , DOI: 10.1016/j.jgg.2018.09.006 Wangjie Liu 1 , Huan Wu 2 , Li Wang 3 , Xiaoyu Yang 4 , Chunyu Liu 3 , Xiaojin He 2 , Weiyu Li 3 , Jiajia Wang 2 , Yujie Chen 2 , Hongyan Wang 3 , Yang Gao 2 , Shuyan Tang 3 , Shenmin Yang 5 , Li Jin 3 , Feng Zhang 1 , Yunxia Cao 2
中文翻译:
FSIP2的纯合子功能丧失突变会导致男性不育,并伴有弱精子症。
更新日期:2019-11-01
Journal of Genetics and Genomics ( IF 5.9 ) Pub Date : 2018-12-06 , DOI: 10.1016/j.jgg.2018.09.006 Wangjie Liu 1 , Huan Wu 2 , Li Wang 3 , Xiaoyu Yang 4 , Chunyu Liu 3 , Xiaojin He 2 , Weiyu Li 3 , Jiajia Wang 2 , Yujie Chen 2 , Hongyan Wang 3 , Yang Gao 2 , Shuyan Tang 3 , Shenmin Yang 5 , Li Jin 3 , Feng Zhang 1 , Yunxia Cao 2
Affiliation
中文翻译:
FSIP2的纯合子功能丧失突变会导致男性不育,并伴有弱精子症。