| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 9443868 | 1998 | Howell, N., Bogolin, C., Jamieson, R., Marenda, D.R., Mackey, D.A. (1998) mtDNA mutations that cause optic neuropathy: how do we know? American Journal of Human Genetics . 62 (1): 196-202 . |
| 2 | 11349229 | 2001 | Finnila, S., Lehtonen, M. S., Majamaa, K. (2001) Phylogenetic network for European mtDNA American Journal of Human Genetics . 68 (6): 1475-1484 . |
| 3 | 11406419 | 2001 | Finnila, S., Hassinen, I. E., Majamaa, K. (2001) Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region Mutation Research . 458 (40545): 31-39 . |
| 4 | 15922297 | 2005 | Zhadanov, S. I., Atamanov, V. V., Zhadanov, N. I., Oleinikov, O. V., Osipova, L. P., Schurr, T. G. (2005) A novel mtDNA ND6 gene mutation associated with LHON in a Caucasian family Biochemical and Biophysical Research Communications . 332 (4): 1115-1121 . |
| 5 | NA | 2014 | van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb . |
| 6 | 31152278 | 2020 | Kytovuori, L., Junttila, J., Huikuri, H., Keinanen-Kiukaanniemi, S., Majamaa, K., Martikainen, M. H. (2020) Mitochondrial DNA variation in sudden cardiac death: a population-based study International Journal of Legal Medicine . 134 (1): 39-44 . |