MITOMAP References for RNA Mutation A606G

• Chinnery, P. F., Johnson, M. A., Taylor, R. W., Lightowlers, R. N., Turnbull, D. M. (1997) A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis Annals of Neurology . 41 (3): 408-410 .


• McFarland, R., Taylor, R. W., Chinnery, P. F., Howell, N., Turnbull, D. M. (2004) A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis Neuromuscular Disorders . 14 (2): 162-166 .


• Chinnery, P. F., Elliott, C., Green, G. R., Rees, A., Coulthard, A., Turnbull, D. M., Griffiths, T. D. (2000) The spectrum of hearing loss due to mitochondrial DNA defects Brain . 123 (Pt 1): 82-92 .


• Mostafaie, N., Rossmanith, W., Hombauer, H., Dechat, T., Raffelsberger, T., Bauer, K., Worofka, B., Kittl, E., Hofmann, J., Hejtman, M., Kirchmeyr, W., Schreiber, W., Weissgram, S., Jungwirth, S., Fischer, P., Bittner, R., Huber, K. (2004) Mitochondrial genotype and risk for Alzheimer's disease: cross-sectional data from the Vienna-Transdanube-Aging "VITA" study Journal of Neural Transmission . 111 (9): 1155-1165 .