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6 Possible Causes for RDGB

  • Chromosome 19q13.11 Deletion Syndrome

    PITPNM3 is a human homologue of the Drosophila retinal degeneration (rdgB) protein, which is highly expressed in the retina and has been proposed to be required for membrane[diva-portal.org]

  • Leber Congenital Amaurosis

    Localization of thegeneencodinghuman phosphatidylinositol transfer protein (PITPN) to17p13.3:a gene showing homology to the Drosophilaretinal degeneration B gene (rdgB).[doi.org]

  • Leber Congenital Amaurosis Type 9

    Localization of thegeneencodinghuman phosphatidylinositol transfer protein (PITPN) to17p13.3:a gene showing homology to the Drosophilaretinal degeneration B gene (rdgB).[nature.com]

  • Bardet-Biedl Syndrome Type 11

    Therefore, H-rdgB gene is an attractive candidate for several inherited retinal degenerative diseases [18].[wikigenes.org] Furthermore, using somatic hybrid cell hybridization and fluorescence in situ hybridization H-rdgB gene was mapped to human chromosome 11q13, a region known to contain several[wikigenes.org]

  • Bardet-Biedl Syndrome Typ 5

    Therefore, H-rdgB gene is an attractive candidate for several inherited retinal degenerative diseases [18] .[wikigenes.org] Furthermore, using somatic hybrid cell hybridization and fluorescence in situ hybridization H-rdgB gene was mapped to human chromosome 11q13, a region known to contain several[wikigenes.org]

  • Leber Congenital Amaurosis Typ 14

    Localization of thegeneencodinghuman phosphatidylinositol transfer protein (PITPN) to17p13.3:a gene showing homology to the Drosophilaretinal degeneration B gene (rdgB).[nature.com]

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