Clinical course of cone dystrophy caused by mutations in the RPGR gene.Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.Ultrastructural localization of GPR179, and the impact of mutant forms on retinal function in CSNB1 patients and a mouse model.A gene for X-linked optic atrophy is closely linked to Xp11.4-Xp11.2 region of the X-chromosomeGenotype and phenotype of 101 Dutch patients with congenital stationary night blindness.Cone-rod dystrophy can be a manifestation of Danon disease.
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F.C. Riemslag