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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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| Pubblicato in: | Life (Basel) |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2021
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| Soggetti: | |
| Accesso online: | 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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