| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 1551433 | 1992 | 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 . |
| 2 | 9667787 | 1998 | 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 . |
| 3 | 15313545 | 2004 | 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 . |
| 4 | 16278810 | 2005 | 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 . |
| 5 | 18242646 | 2008 | 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 . |
| 6 | 28296806 | 2018 | 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 . |