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- W1969394703 abstract "Using library to library cross-screening we have identified a number of genomic clones that harbor X-linked sequences expressed in the human choroid/retina. We describe the characterization of one of these, designated XEH.8 (DXS542), which is localized to Xp11.3-q12. Isolation, partial sequencing, and Northern analysis of the cognate cDNA (XEH.8c), has shown that the cDNA has some homology to the dystrophin gene and hybridizes to a 10-kb mRNA present in the choroid and retina but not in fibroblasts. This expressed sequence maps to the same region of the X chromosome as several known X-linked ophthalmic diseases, including Norrie disease, retinitis pigmentosa 2, congenital night blindness and Aland Island eye disease." @default.
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- W1969394703 date "1993-03-01" @default.
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- W1969394703 title "Identification and Partial Characterization of a Candidate Gene for X-Linked Retinopathies Using a Lateral Approach" @default.
- W1969394703 doi "https://doi.org/10.1006/geno.1993.1096" @default.
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