MITOMAP References for RNA Mutation A10044G

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Index PMID Date Reference
1 8888049 1996 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 .
2 10598821 1999 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 .
3 12160969 2002 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 .
4 15466077 2004 Opdal, S. H., Rognum, T. O. (2004) The sudden infant death syndrome gene: does it exist? Pediatrics . 114 (4): e506-512 .
5 15477393 2004 Levinger, L., Morl, M., Florentz, C. (2004) Mitochondrial tRNA 3' end metabolism and human disease Nucleic Acids Research . 32 (18): 5430-5441 .
6 16773565 2006 Saxena, R., de Bakker, P. I., Singer, K., Mootha, V., Burtt, N., Hirschhorn, J. N., Gaudet, D., Isomaa, B., Daly, M. J., Groop, L., Ardlie, K. G., Altshuler, D. (2006) Comprehensive association testing of common mitochondrial DNA variation in metabolic disease American Journal of Human Genetics . 79 (1): 54-61 .
7 16947981 2006 Ruiz-Pesini, E., Wallace, D. C. (2006) Evidence for adaptive selection acting on the tRNA and rRNA genes of the human mitochondrial DNA Human Mutation . 27 (11): 1072-1081 .