| Index | PMID | Date | Reference |
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| 2 | 15638829 | 2005 | Starikovskaya, E. B., Sukernik, R. I., Derbeneva, O. A., Volodko, N. V., Ruiz-Pesini, E., Torroni, A., Brown, M. D., Lott, M. T., Hosseini, S. H., Huoponen, K., Wallace, D. C. (2005) Mitochondrial DNA diversity in indigenous populations of the southern belt of Siberia and its implications for the origins and evolution of Native American haplogroups Annals of Human Genetics . 69 (Pt 1): 67-89 . |
| 3 | 16168391 | 2005 | Zhao, L., Wang, Q., Qian, Y., Li, R., Cao, J., Hart, L. C., Zhai, S., Han, D., Young, W. Y., Guan, M. X. (2005) Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss Biochemical and Biophysical Research Communications . 336 (3): 967-973 . |
| 4 | 16714301 | 2006 | Kong, Q. P., Bandelt, H. J., Sun, C., Yao, Y. G., Salas, A., Achilli, A., Wang, C. Y., Zhong, L., Zhu, C. L., Wu, S. F., Torroni, A., Zhang, Y. P. (2006) Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations Human Molecular Genetics . 15 (13): 2076-2086 . |
| 5 | 17452034 | 2007 | Wei, Q. P., Zhou, X., Yang, L., Sun, Y. H., Zhou, J., Li, G., Jiang, R., Lu, F., Qu, J., Guan, M. X. (2007) The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing loss Biochemical and Biophysical Research Communications . 357 (4): 910-916 . |
| 6 | 17698030 | 2007 | Yuan, H., Chen, J., Liu, X., Cheng, J., Wang, X., Yang, L., Yang, S., Cao, J., Kang, D., Dai, P., Zhai, S., Han, D., Young, W. Y., Guan, M. X. (2007) Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss Biochemical and Biophysical Research Communications . 362 (1): 94-100 . |
| 7 | 19167085 | 2009 | Qu, J., Zhou, X., Zhang, J., Zhao, F., Sun, Y. H., Tong, Y., Wei, Q. P., Cai, W., Yang, L., West, C. E., Guan, M. X. (2009) Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation Ophthalmology . 116 (3): 558-564 e3 . |
| 8 | 19546379 | 2009 | Li, R., Liu, Y., Li, Z., Yang, L., Wang, S., Guan, M. X. (2009) Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family Hypertension . 54 (2): 329-337 . |
| 9 | 19818876 | 2010 | Lu, J., Qian, Y., Li, Z., Yang, A., Zhu, Y., Li, R., Yang, L., Tang, X., Chen, B., Ding, Y., Li, Y., You, J., Zheng, J., Tao, Z., Zhao, F., Wang, J., Sun, D., Zhao, J., Meng, Y., Guan, M. X. (2010) Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation Mitochondrion . 10 (1): 69-81 . |
| 10 | 20627642 | 2010 | Zhou, X., Zhang, H., Zhao, F., Ji, Y., Tong, Y., Zhang, J., Zhang, Y., Yang, L., Qian, Y., Lu, F., Qu, J., Guan, M. X. (2010) Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation Molecular Genetics and Metabolism . 100 (4): 379-384 . |
| 11 | 21741027 | 2011 | Shah, A. M., Tamang, R., Moorjani, P., Rani, D. S., Govindaraj, P., Kulkarni, G., Bhattacharya, T., Mustak, M. S., Bhaskar, L. V., Reddy, A. G., Gadhvi, D., Gai, P. B., Chaubey, G., Patterson, N., Reich, D., Tyler-Smith, C., Singh, L., Thangaraj, K. (2011) Indian Siddis: African descendants with Indian admixture American Journal of Human Genetics . 89 (1): 154-161 . |
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| 13 | 21978175 | 2011 | Kumar, S., Bellis, C., Zlojutro, M., Melton, P. E., Blangero, J., Curran, J. E. (2011) Large scale mitochondrial sequencing in Mexican Americans suggests a reappraisal of Native American origins BMC Evolutionary Biology . 11 (): 293 . |
| 14 | 23254936 | 2013 | Paull, D., Emmanuele, V., Weiss, K. A., Treff, N., Stewart, L., Hua, H., Zimmer, M., Kahler, D. J., Goland, R. S., Noggle, S. A., Prosser, R., Hirano, M., Sauer, M. V., Egli, D. (2013) Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants Nature . 493 (7434): 632-637 . |
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| 16 | NA | 2014 | van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb . |
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