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pubmed-article:10589235pubmed:abstractTextChoroideremia is an X-linked hereditary eye disease that causes progressive degeneration of the choroid and retina and frequently leads to legal blindness in later life. Recent molecular genetic studies have revealed mutations involving the Rab escort protein (REP-1) gene localized at Xq 21.lld:pubmed
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pubmed-article:10589235pubmed:articleTitle[Clinical and genetic features of choroideremia].lld:pubmed
pubmed-article:10589235pubmed:affiliationDepartment of Ophthalmology, Kagoshima University Faculty of Medicine, Japan.lld:pubmed
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