Index | PMID | Date | Reference |
---|---|---|---|
1 | 9380435 | 1997 | Verma, A., Piccoli, D. A., Bonilla, E., Berry, G. T., DiMauro, S., Moraes, C. T. (1997) A novel mitochondrial G8313A mutation associated with prominent initial gastrointestinal symptoms and progressive encephaloneuropathy Pediatric Research . 42 (4): 448-454 . |
2 | 12737626 | 2003 | Bacman, S. R., Atencio, D. P., Moraes, C. T. (2003) Decreased mitochondrial tRNALys steady-state levels and aminoacylation are associated with the pathogenic G8313A mitochondrial DNA mutation Biochemical Journal . 374 (Pt 1): 131-136 . |
3 | 15100439 | 2004 | Sissler, M., Helm, M., Frugier, M., Giege, R., Florentz, C. (2004) Aminoacylation properties of pathology-related human mitochondrial tRNA(Lys) variants RNA . 10 (5): 841-853 . |
4 | 15477393 | 2004 | Levinger, L., Morl, M., Florentz, C. (2004) Mitochondrial tRNA 3' end metabolism and human disease Nucleic Acids Research . 32 (18): 5430-5441 . |
5 | 19618438 | 2009 | O'Rourke, K., Buddles, M. R., Farrell, M., Howley, R., Sukuraman, S., Connolly, S., Turnbull, D. M., Hutchinson, M., Taylor, R. W. (2009) Phenotypic diversity associated with the mitochondrial m.8313G>A point mutation Muscle and Nerve . 40 (4): 648-651 . |