Related references
Note: Only part of the references are listed.The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype
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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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Mitochondrial fusion protects against neurodegeneration in the cerebellum
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The Charcot-Marie-Tooth type 2A gene product, Mfn2, up-regulates fuel oxidation through expression of OXPHOS system
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Two direct repeats cause most human mtDNA deletions
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Structural basis of mitochondrial tethering by mitofusin complexes
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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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