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Congenital stationary night blindness (CSNB) is a nonprogressive retinaldisorder that can be associated with impaired night vision.
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Achromatopsia is an inherited retinaldisorder of cone photoreceptors characterized by markedly reduced visual acuity, extreme light sensitivity, and absence of color discrimination.
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Congenital stationary night blindness (CSNB) is a clinically and genetically heterogeneous group of non-progressive retinaldisorder with largely normal fundus appearance.
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Degeneration of RPE cells results in retinaldisorders such as age-related macular degeneration.
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Mutations in ABCA4 cause Stargardt disease and other blinding autosomal recessive retinaldisorders.
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The third project is exploring the development of gene therapies for common retinaldisorders.
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Eye burn was the cause of corneal and retinaldisorders in another four cases.
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The development of therapies for retinaldisorders is hampered by a lack of appropriate animal models.
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Retinaldisorders seem to be increasing in importance while childhood disorders have declined over a period of 10 years.
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The identified exon-intron structure of cRPGRIP1 isoforms provides a basis for evaluating the gene defects underlying inherited retinaldisorders in dogs.
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It also said planning to make regulatory submission for microplasmin (for retinaldisorders) in the U.S. and Europe by mid 2011.
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The retina-specific expression and the sequence similarity to RP1 render RP1L1 a potential candidate for inherited retinaldisorders.