| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 16955414 | 2006 | Feigenbaum, A., Bai, R. K., Doherty, E. S., Kwon, H., Tan, D., Sloane, A., Cutz, E., Robinson, B. H., Wong, L. J. (2006) Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness American Journal of Medical Genetics. Part A . 140 (20): 2216-2222 . |
| 2 | 29976239 | 2018 | Tseng, C. C., Chen, C. J., Yen, J. H., Huang, H. Y., Chang, J. G., Chang, S. J., Liao, W. T. (2018) Next-generation sequencing profiling of mitochondrial genomes in gout Arthritis Research and Therapy . 20 (1): 137 . |
| 3 | 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 . |
| 4 | 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 . |