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Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a mitochondrial disorder associated with heteroplasmic point mutations in the mitochondrial tRNA(Leu)(UUR) gene. While previous studies have shown that the MELAS mutation at nt-3243 results in impairments in...
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| Publicado no: | Nucleic Acids Res |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
1993
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| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC309166/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7680123/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/21.3.657 |
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