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pubmed-article:16319817pubmed:abstractTextThe purpose of this paper is to map the locus for a variant form of Oguchi disease in a Pakistani family and to identify the causative mutation.lld:pubmed
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pubmed-article:16319817pubmed:articleTitleA variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.lld:pubmed
pubmed-article:16319817pubmed:affiliationOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892-1860, USA. zhang-q@gzsums.edu.cnlld:pubmed
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