Index | PMID | Date | Reference |
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1 | 16060290 | 2005 | Guo, L. J., Oshida, Y., Fuku, N., Takeyasu, T., Fujita, Y., Kurata, M., Sato, Y., Ito, M., Tanaka, M. (2005) Mitochondrial genome polymorphisms associated with type-2 diabetes or obesity Mitochondrion . 5 (1): 15-33 . |
2 | 20643099 | 2010 | Zou, Y., Jia, X., Zhang, A. M., Wang, W. Z., Li, S., Guo, X., Kong, Q. P., Zhang, Q., Yao, Y. G. (2010) The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations Biochemical and Biophysical Research Communications . 399 (2): 179-185 . |
3 | 21144833 | 2011 | Chamkha, I., Mkaouar-Rebai, E., Aloulou, H., Chabchoub, I., Kifagi, C., Fendri-Kriaa, N., Kammoun, T., Hachicha, M., Fakhfakh, F. (2011) A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNA(Ile) m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss Biochemical and Biophysical Research Communications . 404 (1): 504-510 . |
4 | 23301511 | 2013 | Mkaouar-Rebai, E., Chamkha, I., Mezghani, N., Ben Ayed, I., Fakhfakh, F. (2013) Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: an overview study Mitochondrial DNA . 24 (3): 163-178 . |
5 | 23847141 | 2013 | Bannwarth, S., Procaccio, V., Lebre, A. S., Jardel, C., Chaussenot, A., Hoarau, C., Maoulida, H., Charrier, N., Gai, X., Xie, H. M., Ferre, M., Fragaki, K., Hardy, G., Mousson de Camaret, B., Marlin, S., Dhaenens, C. M., Slama, A., Rocher, C., Paul Bonnefont, J., Rotig, A., Aoutil, N., Gilleron, M., Desquiret-Dumas, V., Reynier, P., Ceresuela, J., Jonard, L., Devos, A., Espil-Taris, C., Martinez, D., Gaignard, P., Le Quan Sang, K. H., Amati-Bonneau, P., Falk, M. J., Florentz, C., Chabrol, B., Durand-Zaleski, I., Paquis-Flucklinger, V. (2013) Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders Journal of Medical Genetics . 50 (10): 704-714 . |
6 | 28139165 | 2017 | Soldath, P., Wegener, M., Sander, B., Rosenberg, T., Duno, M., Wibrand, F., Vissing, J. (2017) Leber hereditary optic neuropathy due to a new ND1 mutation Ophthalmic Genetics . 38 (5): 480-485 . |
7 | 32011699 | 2020 | Gutierrez Cortes, N., Pertuiset, C., Dumon, E., Borlin, M., Da Costa, B., Le Guedard, M., Stojkovic, T., Loundon, N., Rouillon, I., Nadjar, Y., Letellier, T., Jonard, L., Marlin, S., Rocher, C. (2020) Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestations Human Molecular Genetics . 29 (6): 980-989 . |
8 | 32652755 | 2020 | Wong, L. C., Chen, T., Schmitt, E. S., Wang, J., Tang, S., Landsverk, M., Li, F., Zhang, S., Wang, Y., Zhang, V. W., Craigen, W. J. (2020) Clinical and laboratory interpretation of mitochondrial mRNA variants Human Mutation . 41 (10): . |
9 | 36431069 | 2022 | Alkhaldi, H. A., Phan, D. H., Vik, S. B. (2022) Analysis of human clinical mutations of mitochondrial ND1 in a bacterial model system for complex I Life . 12 (11): 1934 . |