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A Novel Mutation in the XLRS1 Gene in a Korean Family with X-linked Retinoschisis

Koh HJ, Jwa NS, Kim SS, Lee SC, Kwon OW

PURPOSE: To report a novel missense mutation in the XLRS1 gene in a Korean family with X-linked retinoschisis. METHODS: Observation case report of a family with a proband with...
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