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OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion
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Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions:: a novel disorder of mtDNA maintenance
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Expression of the Opa1 mitochondrial protein in retinal ganglion cells:: Its downregulation causes aggregation of the mitochondrial network
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Severe impairment of complex I-Driven adenosine triphosphate synthesis in Leber hereditary optic neuropathy cybrids
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eOPA1:: An online database for OPA1 mutations
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OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brain
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The distributions of mitochondria and sodium channels reflect the specific energy requirements and conduction properties of the human optic nerve head
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Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia:: A syndrome caused by a missense mutation in OPA1
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Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy
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OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance
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Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiency
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Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy
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OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
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