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Increased Protein S-Glutathionylation in Leber’s Hereditary Optic Neuropathy (LHON)
Leber’s hereditary optic neuropathy (LHON, MIM#535000) is the most common form of inherited optic neuropathies and mitochondrial DNA-related diseases. The pathogenicity of mutations in genes encoding components of mitochondrial Complex I is well established, but the underlying pathomechanisms of the...
Tallennettuna:
| Julkaisussa: | Int J Mol Sci |
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| Päätekijät: | , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7215361/ https://ncbi.nlm.nih.gov/pubmed/32344771 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21083027 |
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