Index | PMID | Date | Reference |
---|---|---|---|
1 | 16624503 | 2006 | Li, R., Qu, J., Zhou, X., Tong, Y., Hu, Y., Qian, Y., Lu, F., Mo, J. Q., West, C. E., Guan, M. X. (2006) The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family Gene . 376 (1): 79-86 . |
2 | 19022198 | 2008 | Cai, W., Fu, Q., Zhou, X., Qu, J., Tong, Y., Guan, M. X. (2008) Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation Journal of Genetics and Genomics . 35 (11): 649-655 . |
3 | 21983721 | 2011 | Zhang, Y., Zhang, J. J., Ji, Y. C., Zhang, M. L., Tong, Y., Zhao, F. X., Qu, J., Zhou, X. T., Guan, M. X. (2011) [The mitochondrial tRNA(Thr) A15951G mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families] Zhonghua Yi Xue Yi Chuan Xue Za Zhi . 28 (5): 501-506 . |
4 | 23563965 | 2013 | Levin, L., Zhidkov, I., Gurman, Y., Hawlena, H., Mishmar, D. (2013) Functional recurrent mutations in the human mitochondrial phylogeny: dual roles in evolution and disease Genome Biology and Evolution . 5 (5): 876-890 . |
5 | 26000946 | 2016 | Zhang, X., Yu, S., Tu, Y., Huang, W. (2016) Mitochondrial tRNA(Thr) A15951G mutation may not be associated with Leber's hereditary optic neuropathy Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis . 27 (4): 2323-2325 . |
6 | 29387390 | 2018 | Dai, Y., Wang, C., Nie, Z., Han, J., Chen, T., Zhao, X., Ai, C., Ji, Y., Gao, T., Jiang, P. (2018) Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel Biomedical Reports . 8 (1): 51-58 . |