MITOMAP References for Variant T5728C at 5728

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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 .
4	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 .