| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 10369889 | 1999 | Grasbon-Frodl, E. M., Kosel, S., Sprinzl, M., von Eitzen, U., Mehraein, P., Graeber, M. B. (1999) Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease Neurogenetics . 2 (2): 121-127 . |
| 2 | 31965079 | 2020 | Wong, L. C., Chen, T., Wang, J., Tang, S., Schmitt, E. S., Landsverk, M., Li, F., Wang, Y., Zhang, S., Zhang, V. W., Craigen, W. J. (2020) Interpretation of mitochondrial tRNA variants Genetics in Medicine 22 (5): 917-926; Suppl Table 1 . |
| 3 | 33289513 | 2020 | Jiang, P., Ling, Y., Zhu, T., Luo, X., Tao, Y., Meng, F., Cheng, W., Ji, Y. (2020) Mitochondrial tRNA mutations in Chinese children with tic disorders Bioscience Reports . 40 (12): BSR20201856 . |
| 4 | 35808913 | 2022 | Vela-Sebastian, A., Lopez-Gallardo, E., Emperador, S., Hernandez-Ainsa, C., Pacheu-Grau, D., Blanco, I., Ros, A., Pascual-Benito, E., Rabaneda-Lombarte, N., Presas-Rodriguez, S., Garcia-Robles, P., Montoya, J., Ruiz-Pesini, E. (2022) Toxic and nutritional factors trigger Leber hereditary optic neuropathy due to a mitochondrial tRNA mutation Clinical Genetics . 102 (4): 339-344 . |