| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 9344764 | 1997 | Li, Y. Y., Maisch, B., Rose, M. L., Hengstenberg, C. (1997) Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy Journal of Molecular and Cellular Cardiology . 29 (10): 2699-2709 . |
| 2 | 20153673 | 2010 | Tang, X., Li, R., Zheng, J., Cai, Q., Zhang, T., Gong, S., Zheng, W., He, X., Zhu, Y., Xue, L., Yang, A., Yang, L., Lu, J., Guan, M. X. (2010) Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family Molecular Genetics and Metabolism . 100 (1): 57-64 . |
| 3 | 28990081 | 2017 | Ji, Y., Qiao, L., Liang, X., Zhu, L., Gao, Y., Zhang, J., Jia, Z., Wei, Q. P., Liu, X., Jiang, P., Guan, M. X. (2017) Leber's hereditary optic neuropathy is potentially associated with a novel m.5587T>C mutation in two pedigrees Molecular Medicine Reports . 16 (6): 8997-9004 . |
| 4 | 30783460 | 2019 | Lin, L., Cui, P., Qiu, Z., Wang, M., Yu, Y., Wang, J., Sun, Q., Zhao, H. (2019) The mitochondrial tRNA(Ala) 5587T>C and tRNA(Leu(CUN)) 12280A>G mutations may be associated with hypertension in a Chinese family Experimental and Therapeutic Medicine 17 (3): 1855-1862 . |