Index | PMID | Date | Reference |
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1 | 12612282 | 2003 | Uusimaa, J., Finnila, S., Vainionpaa, L., Karppa, M., Herva, R., Rantala, H., Hassinen, I. E., Majamaa, K. (2003) A mutation in mitochondrial DNA-encoded cytochrome c oxidase II gene in a child with Alpers-Huttenlocher-like disease Pediatrics . 111 (3): e262-e268 . |
2 | 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): . |