Fig. 1
From: Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred
a Israeli-Bedouin kindred affected with LCA. Solid and open symbols represent affected and unaffected individuals, respectively. b Color (top) and red free (bottom) fundus photographs of patient 40. Left panels – right eye. Right panels– left eye. Please note normal fundus appearance in both eyes (except for mild vessel tortuosity) in the presence of very poor vision and extinct ERG response