1. Xu, Weilong, Yao, Zhoujuan, Li, Yunzhi, Wang, Fengsong, Zhang, Hui. 2023. Loss of PMFBP1 Disturbs Mouse Spermatogenesis by Downregulating HDAC3 Expression. In Journal of assisted reproduction and genetics, 40, 1865-1879. doi:10.1007/s10815-023-02874-0. https://pubmed.ncbi.nlm.nih.gov/37423931/
2. Zhu, Fuxi, Liu, Chao, Wang, Fengsong, Cao, Yunxia, Li, Wei. 2018. Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome. In American journal of human genetics, 103, 188-199. doi:10.1016/j.ajhg.2018.06.010. https://pubmed.ncbi.nlm.nih.gov/30032984/
3. Lu, Mengmeng, Kong, Shuai, Xiang, Mingfei, Cao, Yunxia, Zhu, Fuxi. 2021. A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome. In Journal of assisted reproduction and genetics, 38, 949-955. doi:10.1007/s10815-021-02075-7. https://pubmed.ncbi.nlm.nih.gov/33484382/
4. Sha, Yan-Wei, Wang, Xiong, Xu, Xiaohui, You, Min, Wu, Jian-Feng. 2018. Biallelic mutations in PMFBP1 cause acephalic spermatozoa. In Clinical genetics, 95, 277-286. doi:10.1111/cge.13461. https://pubmed.ncbi.nlm.nih.gov/30298696/
5. Deng, Tian-Qin, Xie, Yu-Li, Pu, Jiang-Bo, Xuan, Jiang, Li, Xue-Mei. . Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome: A case report. In World journal of clinical cases, 10, 12761-12767. doi:10.12998/wjcc.v10.i34.12761. https://pubmed.ncbi.nlm.nih.gov/36579083/
6. Arora, Manvi, Mehta, Poonam, Sethi, Shruti, Samara, Mary, Singh, Rajender. 2024. Genetic etiological spectrum of sperm morphological abnormalities. In Journal of assisted reproduction and genetics, 41, 2877-2929. doi:10.1007/s10815-024-03274-8. https://pubmed.ncbi.nlm.nih.gov/39417902/
智鼠故事 
