Index | PMID | Date | Reference |
---|---|---|---|
1 | 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 . |
2 | 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 . |
3 | 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 . |