OPA1 mutations induce mitochondrial DNA instability and optic atrophy â–˜plusâ–™ phenotypes

By Amati-Bonneau Patrizia  

Brain, Vol. 131, Iss. 2, 2008-02 ,pp. : 338-351

Oxford University Press

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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

By Hudson Gavin  

Brain, Vol. 131, Iss. 2, 2008-02 ,pp. : 329-337

Oxford University Press

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`Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation

By Lodi R.  

Brain, Vol. 123, Iss. 9, 2000-09 ,pp. : 1896-1902

Oxford University Press

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Opa1 deficiency in a mouse model of dominant optic atrophy leads to retinal ganglion cell dendropathy

By Williams Pete A.  

Brain, Vol. 133, Iss. 10, 2010-10 ,pp. : 2942-2951

Oxford University Press

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OPA1 mutations and mitochondrial DNA damage: keeping the magic circle in shape

By Zeviani Massimo  

Brain, Vol. 131, Iss. 2, 2008-02 ,pp. : 314-317

Oxford University Press

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