1. Ding, Yuxi, Chen, Shuya, Jin, Jing, Xin, Mingwei, Li, Lin. 2024. POI-associated EIF4ENIF1 mutations exhibit impaired translation regulation abilities. In Gene, 917, 148456. doi:10.1016/j.gene.2024.148456. https://pubmed.ncbi.nlm.nih.gov/38604507/
2. Shang, Lingyue, Ren, Shuting, Yang, Xi, Zhang, Xiaojin, Wu, Yanhua. 2022. EIF4ENIF1 variants in two patients with non-syndromic premature ovarian insufficiency. In European journal of medical genetics, 65, 104597. doi:10.1016/j.ejmg.2022.104597. https://pubmed.ncbi.nlm.nih.gov/36030004/
3. Liang, Manqi, Suresh, Beena, Bareke, Eric, Majewski, Jacek, Slim, Rima. . A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage. In Molecular genetics & genomic medicine, 12, e2402. doi:10.1002/mgg3.2402. https://pubmed.ncbi.nlm.nih.gov/38400599/
4. Yang, Ying-zhong, Wang, Ya-ping, Xu, Jin, Ge, Ri-li. . The susceptibility gene screening in a Chinese high-altitude pulmonary edema family by whole-exome sequencing. In Yi chuan = Hereditas, 39, 135-142. doi:10.16288/j.yczz.16-288. https://pubmed.ncbi.nlm.nih.gov/28242600/
5. Ramon Y Cajal, Santiago, Castellvi, Josep, Hümmer, Stefan, Pelletier, Jerry, Sonenberg, Nahum. 2018. Beyond molecular tumor heterogeneity: protein synthesis takes control. In Oncogene, 37, 2490-2501. doi:10.1038/s41388-018-0152-0. https://pubmed.ncbi.nlm.nih.gov/29463861/
6. Zhang, Fuquan, Chen, Yaguang, Liu, Chenxing, Wang, Lifang, Zhang, Dai. 2012. Systematic association analysis of microRNA machinery genes with schizophrenia informs further study. In Neuroscience letters, 520, 47-50. doi:10.1016/j.neulet.2012.05.028. https://pubmed.ncbi.nlm.nih.gov/22595464/
7. Zhao, Minying, Feng, Fan, Chu, Chunfang, Yue, Wentao, Li, Lin. 2019. A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing. In Journal of ovarian research, 12, 119. doi:10.1186/s13048-019-0595-0. https://pubmed.ncbi.nlm.nih.gov/31810472/
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