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...

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Bibliografiset tiedot
Julkaisussa:Int J Mol Sci
Päätekijät: Zhou, Lei, Chan, James Chun Yip, Chupin, Stephanie, Gueguen, Naïg, Desquiret-Dumas, Valérie, Koh, Siew Kwan, Li, Jianguo, Gao, Yan, Deng, Lu, Verma, Chandra, Beuerman, Roger W, Chan, Eric Chun Yong, Milea, Dan, Reynier, Pascal
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: MDPI 2020
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Article
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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