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 | 29876471 | 2018 | Lyu, L., Wang, Q., Song, S., Zhou, H., Li, M., Zhou, C., Jiang, Z., Li, L., Lyu, J., Chen, G., Bai, Y. (2018) Dataset of mitochondrial genome variants in oncocytic tumors Data Brief . 17 (): 1149-1152 . |
3 | 32419253 | 2020 | Zereg, E., Chaussenot, A., Morel, G., Bannwarth, S., Sacconi, S., Soriani, M. H., Attarian, S., Cano, A., Pouget, J., Bellance, R., Tranchant, C., Lannes, B., de Paula, A. M., Saadi Ait-El-Mkadem, S., Chafino, B., Berthet, M., Fragaki, K., Paquis-Flucklinger, V., Rouzier, C. (2020) Single-fiber studies for assigning pathogenicity of eight mitochondrial DNA variants associated with mitochondrial diseases Human Mutation . 41 (8): 1394-1406 . |