Index | PMID | Date | Reference |
---|---|---|---|
1 | 10402027 | 1999 | Hadjigeorgiou, G. M., Kim, S. H., Fischbeck, K. H., Andreu, A. L., Berry, G. T., Bingham, P., Shanske, S., Bonilla, E., DiMauro, S. (1999) A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathy Journal of the Neurological Sciences . 164 (2): 153-157 . |
2 | 15477393 | 2004 | Levinger, L., Morl, M., Florentz, C. (2004) Mitochondrial tRNA 3' end metabolism and human disease Nucleic Acids Research . 32 (18): 5430-5441 . |
3 | 23631826 | 2013 | Wang, M., Zhou, X. L., Liu, R. J., Fang, Z. P., Zhou, M., Eriani, G., Wang, E. D. (2013) Multilevel functional and structural defects induced by two pathogenic mitochondrial tRNA mutations Biochemical Journal . 453 (3): 455-465 . |
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 . |