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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Detalles Bibliográficos
Autores principales: Mayorov, Vladimir I, Lowrey, Angela J, Biousse, Valerie, Newman, Nancy J, Cline, Susan D, Brown, Michael D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2547100/
https://www.ncbi.nlm.nih.gov/pubmed/18783614
http://dx.doi.org/10.1186/1471-2091-9-22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2547100/
https://www.ncbi.nlm.nih.gov/pubmed/18783614
http://dx.doi.org/10.1186/1471-2091-9-22

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