Index | PMID | Date | Reference |
---|---|---|---|
1 | 23463613 | 2013 | Tang, S., Wang, J., Zhang, W., Li, F., Landsverk, M., Cui, H., Truong, C., Wang, G., Li, C., Graham, B., Scaglia, F., Schmitt, E. S., Craigen, W. J., Wong, L. C. (2013) Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects Human Mutation . 34 (6): 882-893 Most reported SNVs are not found in the body of the paper itself but are listed in the supplemental information as Unclassified Variants. |
2 | 31743754 | 2020 | Jancic, J., Rovcanin, B., Djuric, V., Pepic, A., Samardzic, J., Nikolic, B., Novakovic, I., Kostic, V. S. (2020) Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentation Mitochondrion . 50 (): 132-138 . |
3 | 32858252 | 2020 | Rucheton, B., Jardel, C., Filaut, S., Amador, M. D. M., Maisonobe, T., Serre, I., Romero, N. B., Leonard-Louis, S., Haraux, F., Lombes, A. (2020) Homoplasmic deleterious MT-ATP6/8 mutations in adult patients Mitochondrion . 55 (): 64-77 . |