Unexpected effect of calcium channel blockers on the optic nerve compartment syndrome
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The genetics of Leber hereditary optic neuropathy - prototype of an inherited optic neuropathy with mitochondrial dysfunction
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A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome C oxidase subunit I
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Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss
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Optic disc excavation in the atrophic stage of Leberʼs hereditary optic neuropathy: comparison with normal tension glaucoma
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