1. Ramond, Francis, Dalgliesh, Caroline, Grimmel, Mona, Haack, Tobias, Elliott, David J. 2022. Clustered variants in the 5' coding region of TRA2B cause a distinctive neurodevelopmental syndrome. In Genetics in medicine : official journal of the American College of Medical Genetics, 25, 100003. doi:10.1016/j.gim.2022.100003. https://pubmed.ncbi.nlm.nih.gov/36549593/
2. Karginov, Timofey A, Ménoret, Antoine, Leclair, Nathan K, Zhou, Beiyan, Vella, Anthony T. 2024. Autoregulated splicing of TRA2β programs T cell fate in response to antigen-receptor stimulation. In Science (New York, N.Y.), 385, eadj1979. doi:10.1126/science.adj1979. https://pubmed.ncbi.nlm.nih.gov/39265028/
3. Li, Fei, Fang, Zhaoyuan, Zhang, Jian, Chen, Haiquan, Ji, Hongbin. 2016. Identification of TRA2B-DNAH5 fusion as a novel oncogenic driver in human lung squamous cell carcinoma. In Cell research, 26, 1149-1164. doi:10.1038/cr.2016.111. https://pubmed.ncbi.nlm.nih.gov/27670699/