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mt tRFs, New Players in MELAS Disease
MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes) is an OXPHOS disease mostly caused by the m.3243A>G mutation in the mitochondrial tRNA(Leu(UUR)) gene. Recently, we have shown that the mutation significantly changes the expression pattern of several mitochondrial...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8902416/ https://www.ncbi.nlm.nih.gov/pubmed/35273517 http://dx.doi.org/10.3389/fphys.2022.800171 |