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Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease
Point mutations in the mitochondrial (mt) tRNA(Leu(UUR)) gene are responsible for mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS), a subgroup of mitochondrial encephalomyopathic diseases. We previously showed that mt tRNA(Leu(UUR)) with an A3243G or T3271C m...
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| Hoofdauteurs: | , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
National Academy of Sciences
2004
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC524061/ https://ncbi.nlm.nih.gov/pubmed/15477592 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0405173101 |
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