Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia | |
Wangjie Liu; Huan Wu; Li Wang; Xiaoyu Yang; Chunyu Liu; Xiaojin He; Weiyu Li; Jiajia Wang; Yujie Chen; Hongyan Wang | |
刊名 | Journal of Genetics and Genomics |
2019 | |
卷号 | Vol.46 No.1页码:53-56 |
ISSN号 | 1673-8527 |
URL标识 | 查看原文 |
公开日期 | [db:dc_date_available] |
内容类型 | 期刊论文 |
URI标识 | http://www.corc.org.cn/handle/1471x/4747259 |
专题 | 湖南大学 |
作者单位 | 1.b Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, 211116, China a Obstetrics and Gynecology Hospital, NHC Key Laboratory of Reproduction Regulation , School of Life Sciences, Fudan University, Shanghai, 200011, China 2.Reproductive Medicine Center, Department of Obstetrics and Gynecology, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, China 3.Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, Shanghai, 200011, China f Anhui Provincial Engineering Technology Research Center for Biopreservation and Artificial Organs, Hefei, 230022, China 4.Anhui Province Key Laboratory of Reproductive Health and Genetics, Anhui Medical University, Hefei, 230022, China h Center for Reproduction and Genetics, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, 215002, China g Clinical Center of Reproductive Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China |
推荐引用方式 GB/T 7714 | Wangjie Liu,Huan Wu,Li Wang,et al. Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia[J]. Journal of Genetics and Genomics,2019,Vol.46 No.1:53-56. |
APA | Wangjie Liu.,Huan Wu.,Li Wang.,Xiaoyu Yang.,Chunyu Liu.,...&Yunxia Cao.(2019).Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia.Journal of Genetics and Genomics,Vol.46 No.1,53-56. |
MLA | Wangjie Liu,et al."Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia".Journal of Genetics and Genomics Vol.46 No.1(2019):53-56. |
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