Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred

Overview of attention for article published in BMC Medical Genomics, July 2016

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Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred. https://t.co/JtwOQJ5rMw

Report on phenotypic variability among Bedouin-Israeli family affected by LCA1 due to GUCY2D mutation. https://t.co/xHLCXa9Hud #bmcmedgenet

Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a lar... https://t.co/H6GjZxt2wz #Medical #Genetics

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