MITOMAP References for RNA Mutation T5728C

Download PMID list

Index PMID Date Reference
1 23847141 2013 Bannwarth, S., Procaccio, V., Lebre, A. S., Jardel, C., Chaussenot, A., Hoarau, C., Maoulida, H., Charrier, N., Gai, X., Xie, H. M., Ferre, M., Fragaki, K., Hardy, G., Mousson de Camaret, B., Marlin, S., Dhaenens, C. M., Slama, A., Rocher, C., Paul Bonnefont, J., Rotig, A., Aoutil, N., Gilleron, M., Desquiret-Dumas, V., Reynier, P., Ceresuela, J., Jonard, L., Devos, A., Espil-Taris, C., Martinez, D., Gaignard, P., Le Quan Sang, K. H., Amati-Bonneau, P., Falk, M. J., Florentz, C., Chabrol, B., Durand-Zaleski, I., Paquis-Flucklinger, V. (2013) Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders Journal of Medical Genetics . 50 (10): 704-714 .
2 31965079 2020 Wong, L. C., Chen, T., Wang, J., Tang, S., Schmitt, E. S., Landsverk, M., Li, F., Wang, Y., Zhang, S., Zhang, V. W., Craigen, W. J. (2020) Interpretation of mitochondrial tRNA variants Genetics in Medicine 22 (5): 917-926; Suppl Table 1 .
3 16908752 2006 Meulemans, A., Seneca, S., Lagae, L., Lissens, W., De Paepe, B., Smet, J., Van Coster, R., De Meirleir, L. (2006) A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failure Archives of Neurology . 63 (8): 1194-1198 .
4 31026515 2019 Tarnopolsky, M., Brady, L., MacNeil, L. (2019) Myasthenia graves-like symptoms associated with rare mitochondrial mutation (m.5728T>C) Mitochondrion . 47 (): 139-140 .