MITOMAP References for RNA Mutation A10044G

• Santorelli, F. M., Schlessel, J. S., Slonim, A. E., DiMauro, S. (1996) Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death Pediatric Neurology . 15 (2): 145-149 .


• Opdal, S. H., Vege, A., Egeland, T., Musse, M. A., Rognum, T. O. (2002) Possible role of mtDNA mutations in sudden infant death Pediatric Neurology . 27 (1): 23-29 .


• Levinger, L., Morl, M., Florentz, C. (2004) Mitochondrial tRNA 3' end metabolism and human disease Nucleic Acids Research . 32 (18): 5430-5441 .


• Lehtonen, M. S., Meinila, M., Hassinen, I. E., Majamaa, K. (1999) Haplotype-matched controls as a tool to discriminate polymorphisms from pathogenic mutations in mtDNA Human Genetics . 105 (5): 513-514 .


• Opdal, S. H., Rognum, T. O. (2004) The sudden infant death syndrome gene: does it exist? Pediatrics . 114 (4): e506-512 .