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Dec 6, 2022 (publication date) through Nov 3, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Deng TQ, Xie YL, Pu JB, Xuan J, Li XM. Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome: A case report. World J Clin Cases 2022; 10(34): 12761-12767 [PMID: 36579083 DOI: 10.12998/wjcc.v10.i34.12761] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i34/12761.htm |
| Number | Citing Articles |
| 1 |
Thomas Greither, Mario Dejung, Hermann M. Behre, Falk Butter, Holger Herlyn. The human sperm proteome—Toward a panel for male fertility testing. Andrology 2023; 11(7): 1418 doi: 10.1111/andr.13431
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| 2 |
Manvi Arora, Poonam Mehta, Shruti Sethi, George Anifandis, Mary Samara, Rajender Singh. Genetic etiological spectrum of sperm morphological abnormalities. Journal of Assisted Reproduction and Genetics 2024; doi: 10.1007/s10815-024-03274-8
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| 3 |
Weilong Xu, Zhoujuan Yao, Yunzhi Li, Ke Wang, Shuai Kong, Yu Wang, Mingfei Xiang, Fuxi Zhu, Fengsong Wang, Hui Zhang. Loss of PMFBP1 Disturbs Mouse Spermatogenesis by Downregulating HDAC3 Expression. Journal of Assisted Reproduction and Genetics 2023; 40(8): 1865 doi: 10.1007/s10815-023-02874-0
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