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Published in 2023 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms24032679
Abstract: In 25% of patients with mitochondrial myopathies, pathogenic mitochondrial DNA (mtDNA) mutation are the cause. For heteroplasmic mtDNA mutations, symptoms manifest when the mutation load exceeds a tissue-specific threshold. Therefore, lowering the mutation load is…
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Keywords:
mutation load;
mtdna mutation;
type mesoangioblasts;
mutation ... See more keywords