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Mitochondrial tRNA(Ala) 5601C>T variant may affect the clinical expression of the LHON-related ND4 11778G>A mutation in a family
Certain mutations in mitochondrial DNA (mtDNA) are associated with Leber's hereditary optic neuropathy (LHON). In particular, the well-known NADH dehydrogenase 4 (ND4) m.11778G>A mutation is one of the most common LHON-associated primary mutations worldwide. However, how specific mtDNA mutat...
Tallennettuna:
| Julkaisussa: | Mol Med Rep |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
D.A. Spandidos
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6896293/ https://ncbi.nlm.nih.gov/pubmed/31939618 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2019.10844 |
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