1. Larcher, Lise, Buratti, Julien, Héron-Longe, Bénédicte, Keren, Boris, Delahaye-Duriez, Andrée. 2020. New evidence that biallelic loss of function in EEF1B2 gene leads to intellectual disability. In Clinical genetics, 97, 639-643. doi:10.1111/cge.13688. https://pubmed.ncbi.nlm.nih.gov/31845318/
2. Gong, Pan, Liu, Jing, Jiao, Xianru, Wang, Xiaodong, Yang, Zhixian. 2022. Novel biallelic loss of EEF1B2 function links to autosomal recessive intellectual disability. In Human mutation, 43, 299-304. doi:10.1002/humu.24329. https://pubmed.ncbi.nlm.nih.gov/35015920/
3. Huang, Zenghui, Li, Ning, Ji, Xiren, Huang, Chuan, Lin, Ge. 2024. EEF1B2 regulates the proliferation and apoptosis of human spermatogonial stem cell lines through TAF4B. In Heliyon, 10, e36467. doi:10.1016/j.heliyon.2024.e36467. https://pubmed.ncbi.nlm.nih.gov/39281470/
4. Uchida, Shotaro, Sato, Hiroki, Yoneda, Misako, Kai, Chieko. 2016. Eukaryotic elongation factor 1-beta interacts with the 5' untranslated region of the M gene of Nipah virus to promote mRNA translation. In Archives of virology, 161, 2361-8. doi:10.1007/s00705-016-2903-y. https://pubmed.ncbi.nlm.nih.gov/27236461/
5. He, Cuitong, Guo, Jiangtao, Tian, Wenmin, Wong, Catherine C L. 2021. Proteogenomics Integrating Novel Junction Peptide Identification Strategy Discovers Three Novel Protein Isoforms of Human NHSL1 and EEF1B2. In Journal of proteome research, 20, 5294-5303. doi:10.1021/acs.jproteome.1c00373. https://pubmed.ncbi.nlm.nih.gov/34420305/