Index | PMID | Date | Reference |
---|---|---|---|
1 | 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 . |
2 | 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 . |