MITOMAP References for mtDNA Deletion: 8482:13460 -4977 D, 13/13 8470-8482/13447-13459 3

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1551433 Zhang, C., Baumer, A., Maxwell, R. J., Linnane, A. W., Nagley, P. (1992) Multiple mitochondrial DNA deletions in an elderly human individual FEBS Letters . 297 (40545): 34-38 .
9667787 Mohri, I., Taniike, M., Fujimura, H., Matsuoka, T., Inui, K., Nagai, T., Okada, S. (1998) A case of Kearns-Sayre syndrome showing a constant proportion of deleted mitochondrial DNA in blood cells during 6 years of follow-up Journal of the Neurological Sciences . 158 (1): 106-109 .
15313545 Samuels, D. C., Schon, E. A., Chinnery, P. F. (2004) Two direct repeats cause most human mtDNA deletions Trends in Genetics . 20 (9): 393-398 .
16278810 Lebrecht, D., Kokkori, A., Ketelsen, U. P., Setzer, B., Walker, U. A. (2005) Tissue-specific mtDNA lesions and radical-associated mitochondrial dysfunction in human hearts exposed to doxorubicin Journal of Pathology . 207 (4): 436-244 .
18242646 Markaryan, A., Nelson, E. G., Hinojosa, R. (2008) Detection of mitochondrial DNA deletions in the cochlea and its structural elements from archival human temporal bone tissue Mutation Research . 640 (40545): 38-45 .
28296806 Kozak, I., Oystreck, D. T., Abu-Amero, K. K., Nowilaty, S. R., Alkhalidi, H., Elkhamary, S. M., Mohamed, S., Hamad, M. H. A., Salih, M. A., Blakely, E. L., Taylor, R. W., Bosley, T. M. (2018) New observations regarding the retinopathy of genetically confirmed Kearns-Sayre Syndrome Retinal Cases and Brief Reports . 12 (4): 349-358 .
29283441 Rocha, M. C., Rosa, H. S., Grady, J. P., Blakely, E. L., He, L., Romain, N., Haller, R. G., Newman, J., McFarland, R., Ng, Y. S., Gorman, G. S., Schaefer, A. M., Tuppen, H. A., Taylor, R. W., Turnbull, D. M. (2018) Pathological mechanisms underlying single large-scale mitochondrial DNA deletions Annals of Neurology . 83 (1): 115-130 .
32220313 Russell, O. M., Gorman, G. S., Lightowlers, R. N., Turnbull, D. M. (2020) Mitochondrial diseases: hope for the future Cell . 181 (1): 168-188 .