MITOMAP References for RNA Mutation T5587C

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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 .