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2. Tresky, Roland, Miyamoto, Yuta, Nagayoshi, Yu, Tomizawa, Kazuhito, Chujo, Takeshi. . TRMT10A dysfunction perturbs codon translation of initiator methionine and glutamine and impairs brain functions in mice. In Nucleic acids research, 52, 9230-9246. doi:10.1093/nar/gkae520. https://pubmed.ncbi.nlm.nih.gov/38950903/
3. Samhani, C, Guerci, B, Larose, C. 2024. Discovery of a TRMT10A mutation in a case of atypical diabetes: Case report. In Diabetes & metabolism, 50, 101572. doi:10.1016/j.diabet.2024.101572. https://pubmed.ncbi.nlm.nih.gov/39243962/
4. Stern, Eve, Vivante, Asaf, Barel, Ortal, Levy-Shraga, Yael. 2021. TRMT10A Mutation in a Child with Diabetes, Short Stature, Microcephaly and Hypoplastic Kidneys. In Journal of clinical research in pediatric endocrinology, 14, 227-232. doi:10.4274/jcrpe.galenos.2020.2020.0265. https://pubmed.ncbi.nlm.nih.gov/33448213/
5. Şıklar, Zeynep, Kontbay, Tuğba, Colclough, Kevin, Patel, Kashyap A., Berberoğlu, Merih. 2021. Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases. In Journal of clinical research in pediatric endocrinology, 15, 90-96. doi:10.4274/jcrpe.galenos.2021.2021.0110. https://pubmed.ncbi.nlm.nih.gov/34541035/
6. Ontiveros, R Jordan, Shen, Hui, Stoute, Julian, Zhang, Yuyu, Liu, Kathy Fange. 2020. Coordination of mRNA and tRNA methylations by TRMT10A. In Proceedings of the National Academy of Sciences of the United States of America, 117, 7782-7791. doi:10.1073/pnas.1913448117. https://pubmed.ncbi.nlm.nih.gov/32213595/
7. Lin, Hu, Zhou, Xuelian, Chen, Xuefeng, Polychronakos, Constantin, Dong, Guan-Ping. . tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly. In BMJ open diabetes research & care, 8, . doi:10.1136/bmjdrc-2020-001601. https://pubmed.ncbi.nlm.nih.gov/33067246/
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