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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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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2008
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| Assuntos: | |
| Acesso em linha: | 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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