Shuntaro Oba

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HYPOTHESIS Different missense mutations of the optic atrophy 1 gene (OPA1) identified in optic atrophy patients with auditory neuropathy spectrum disorder (ANSD) induce functional impairment through different molecular mechanisms. BACKGROUND OPA1 is the gene responsible for autosomal dominant optic atrophy (ADOA), but some of its mutations are also(More)
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