Index | PMID | Date | Reference |
---|---|---|---|
1 | 8213825 | 1993 | Howell, N., Halvorson, S., Burns, J., McCullough, D.A., Poulton, J. (1993) When does bilateral optic atrophy become Leber hereditary optic atrophy? American Journal of Human Genetics . 53 (4): 959-963 . |
2 | 7760326 | 1995 | Riordan-Eva, P., Harding, A.E. (1995) Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations Journal of Medical Genetics . 32 (2): 81-87 . |
3 | 8593537 | 1995 | Sartore, M., Grasso, M., Piccolo, G., Fasani, R., Bergamaschi, R., Malaspina, A., Ceroni, M., Kobayashi, M., Semeraro, A., Arbustini, E., Surrey, S., Fortina, P. (1995) Leber's hereditary optic neuropathy (LHON)-related mitochondrial DNA sequence changes in Italian patients presenting with sporadic bilateral optic neuritis Biochemical and Molecular Medicine . 56 (1): 45-51 . |
4 | 8899049 | 1996 | Mayr-Wohlfart, U., Paulus, C., Henneberg, A., Rodel, G. (1996) Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement Acta Neurologica Scandinavica . 94 (3): 167-171 . |
5 | 15972314 | 2006 | Mitchell, A. L., Elson, J. L., Howell, N., Taylor, R. W., Turnbull, D. M. (2006) Sequence variation in mitochondrial complex I genes: mutation or polymorphism? Journal of Medical Genetics . 43 (2): 175-179 . |
6 | 19001017 | 2009 | Yu-Wai-Man, P., Griffiths, P. G., Hudson, G., Chinnery, P. F. (2009) Inherited mitochondrial optic neuropathies [Review] Journal of Medical Genetics . 46 (3): 145-158 . |
7 | 21457906 | 2011 | Pereira, L., Soares, P., Radivojac, P., Li, B., Samuels, D. C. (2011) Comparing phylogeny and the predicted pathogenicity of protein variations reveals equal purifying selection across the global human mtDNA diversity American Journal of Human Genetics . 88 (4): 433-439 . |