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Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy

BACKGROUND: Autosomal dominant optic atrophy (ADOA), a form of progressive bilateral blindness due to loss of retinal ganglion cells and optic nerve deterioration, arises predominantly from mutations in the nuclear gene for the mitochondrial GTPase, OPA1. OPA1 localizes to mitochondrial cristae in t...

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Autori principali: Mayorov, Vladimir I, Lowrey, Angela J, Biousse, Valerie, Newman, Nancy J, Cline, Susan D, Brown, Michael D
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2008
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2547100/
https://ncbi.nlm.nih.gov/pubmed/18783614
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2091-9-22
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