| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 7525879 | 1994 | Hattori, Y., Goto, Y., Sakuta, R., Nonaka, I., Mizuna, Y., Horai, S. (1994) Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO) Journal of the Neurological Sciences . 125 (1): 50-55 . |
| 2 | 7804130 | 1994 | Sato, W., Hayasaka, K., Shoji, Y., Takahashi, T., Takada, G., Saito, M., Fukawa, O., Wachi, E. (1994) A mitochondrial tRNA(Leu)(UUR) mutation at 3256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke- like episodes (MELAS) Biochemistry and Molecular Biology International (Sydney) . 33 (6): 1055-1061 . |
| 3 | 16947981 | 2006 | Ruiz-Pesini, E., Wallace, D. C. (2006) Evidence for adaptive selection acting on the tRNA and rRNA genes of the human mitochondrial DNA Human Mutation . 27 (11): 1072-1081 . |
| 4 | 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 . |