| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 11477557 | 2001 | Kirches, E., Krause, G., Warich-Kirches, M., Weis, S., Schneider, T., Meyer-Puttlitz, B., Mawrin, C., Dietzmann, K. (2001) High frequency of mitochondrial DNA mutations in glioblastoma multiforme identified by direct sequence comparison to blood samples International Journal of Cancer . 93 (4): 534-538 . |
| 2 | 12000737 | 2002 | Maximo, V., Soares, P., Lima, J., Cameselle-Teijeiro, J., Sobrinho-Simoes, M. (2002) Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hurthle cell tumors American Journal of Pathology . 160 (5): 1857-1865 . |
| 3 | 15181170 | 2004 | Wanrooij, S., Luoma, P., van Goethem, G., van Broeckhoven, C., Suomalainen, A., Spelbrink, J. N. (2004) Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA Nucleic Acids Research . 32 (10): 3053-3064 . |
| 4 | 16892079 | 2006 | Brandon, M., Baldi, P., Wallace, D. C. (2006) Mitochondrial mutations in cancer Oncogene . 25 (34): 4647-4662 . |
| 5 | 23077218 | 2013 | Payne, B. A., Wilson, I. J., Yu-Wai-Man, P., Coxhead, J., Deehan, D., Horvath, R., Taylor, R. W., Samuels, D. C., Santibanez-Koref, M., Chinnery, P. F. (2013) Universal heteroplasmy of human mitochondrial DNA Human Molecular Genetics . 22 (2): 384-390 . |