MITOMAP References for RNA Mutation G3242A

• Kirino, Y., Goto, Y. I., Campos, Y., Arenas, J., Suzuki, T. (2005) Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease Proceedings of the National Academy of Sciences of the United States of America . 102 (20): 7127-7132 .


• Mimaki, M., Hatakeyama, H., Ichiyama, T., Isumi, H., Furukawa, S., Akasaka, M., Kamei, A., Komaki, H., Nishino, I., Nonaka, I., Goto, Y. (2009) Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders Mitochondrion . 9 (2): 115-122 .


• Wortmann, S. B., Champion, M. P., van den Heuvel, L., Barth, H., Trutnau, B., Craig, K., Lammens, M., Schreuder, M. F., Taylor, R. W., Smeitink, J. A., Wevers, R. A., Rodenburg, R. J., Morava, E. (2012) Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction? European Journal of Medical Genetics . 55 (10): 552-556 .