Index | PMID | Date | Reference |
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1 | 12736867 | 2003 | Howell, N., Oostra, R. J., Bolhuis, P. A., Spruijt, L., Clarke, L. A., Mackey, D. A., Preston, G., Herrnstadt, C. (2003) Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy American Journal of Human Genetics . 72 (6): 1460-1469 . |
2 | 27164671 | 2016 | Dombi, E., Diot, A., Morten, K., Carver, J., Lodge, T., Fratter, C., Ng, Y. S., Liao, C., Muir, R., Blakely, E. L., Hargreaves, I., Al-Dosary, M., Sarkar, G., Hickman, S. J., Downes, S. M., Jayawant, S., Yu-Wai-Man, P., Taylor, R. W., Poulton, J. (2016) The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy Neurology . 86 (20): 1921-1923 . |