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Exploring the Ability of LARS2 Carboxy-Terminal Domain in Rescuing the MELAS Phenotype
The m.3243A>G mutation within the mitochondrial mt-tRNALeu((UUR)) gene is the most prevalent variant linked to mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome. This pathogenic mutation causes severe impairment of mitochondrial protein synthesis due to a...
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| Publicat a: | Life (Basel) |
|---|---|
| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8303833/ https://ncbi.nlm.nih.gov/pubmed/34357047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/life11070674 |
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