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Structural probing of a pathogenic tRNA dimer
The A3243G mutation within the human mitochondrial (hs mt) tRNA(Leu(UUR)) gene is associated with maternally inherited deafness and diabetes (MIDD) and other mitochondrial encephalopathies. One of the most pronounced structural effects of this mutation is the disruption of the native structure throu...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Copyright 2005 by RNA Society
2005
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1370715/ https://ncbi.nlm.nih.gov/pubmed/15701731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.7143305 |
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