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Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophy
PURPOSE: The majority of patients with autosomal dominant optic atrophy (DOA) harbor pathogenic OPA1 mutations and certain missense mutations, mostly within the GTPase domain, have recently been shown to cause multiple mitochondrial DNA (mtDNA) deletions in skeletal muscle. This raises the possibili...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4034167/ https://ncbi.nlm.nih.gov/pubmed/19443720 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.09-3634 |
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