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Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency
Childhood-onset mitochondrial encephalomyopathies are severe, relentlessly progressive conditions. However, reversible infantile respiratory chain deficiency (RIRCD), due to a homoplasmic mt-tRNA(Glu) mutation, and reversible infantile hepatopathy, due to tRNA 5-methylaminomethyl-2-thiouridylate met...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3889809/ https://ncbi.nlm.nih.gov/pubmed/23814040 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt309 |
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