Index | PMID | Date | Reference |
---|---|---|---|
1 | NA | 2020 | Bolze, A., Mendez, F., White, S., Tanudjaja, F., Isaksson, M., Jiang, R., Dei Rossi, A., Cirulli, E. T., Rashkin, M., Metcalf, W. J., Grzymski, J. J., Lee, W., Lu, J. T. and Washington, N. L. (2020) A catalog of homoplasmic and heteroplasmic mitochondrial DNA variants in humans bioRxiv . ePub (https://www.biorxiv.org/content/10.1101/798264v3): 798264 . |
2 | NA | 2021 | Engvall, M., Kawasaki, A., Carelli, V., Wibom, R., Bruhn, H., Lesko, N., Schober, F. A., Wredenberg, A., Wedell, A., Träisk, F. (2021) Case report: a novel mutation in the mitochondrial MT-ND5 gene Is associated aith Leber hereditary optic neuropathy (LHON) Frontiers in Neurology . 12 (): 391 . |