Yoko Goto-Fukuura

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PURPOSE To determine whether a mutation in the RP1-like protein 1 (RP1L1) gene is present in a Japanese patient with sporadic occult macular dystrophy (OMD) and to examine the characteristics of focal macular electroretinograms (ERGs) of the patient with genetically identified OMD. METHODS An individual with OMD underwent detailed ophthalmic clinical(More)
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