Index | PMID | Date | Reference |
---|---|---|---|
1 | 8910895 | 1996 | Dumoulin, R., Sagnol, I., Ferlin, T., Bozon, D., Stepien, G., Mousson, B. (1996) A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance Molecular and Celllar Probes . 10 (5): 389-391 . |
2 | 8988236 | 1996 | Bouzidi, M. F., Carrier, H., Godinot, C. (1996) Antimycin resistance and ubiquinol cytochrome c reductase instability associated with a human cytochrome b mutation Biochimica et Biophysica Acta . 1317 (3): 199-209 . |
3 | 21457906 | 2011 | Pereira, L., Soares, P., Radivojac, P., Li, B., Samuels, D. C. (2011) Comparing phylogeny and the predicted pathogenicity of protein variations reveals equal purifying selection across the global human mtDNA diversity American Journal of Human Genetics . 88 (4): 433-439 . |
4 | 32652755 | 2020 | Wong, L. C., Chen, T., Schmitt, E. S., Wang, J., Tang, S., Landsverk, M., Li, F., Zhang, S., Wang, Y., Zhang, V. W., Craigen, W. J. (2020) Clinical and laboratory interpretation of mitochondrial mRNA variants Human Mutation . 41 (10): . |