Publisher
Springer Nature Singapore
Reference17 articles.
1. Hamel CP, et al. Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes. J Fr Ophtalmol. 2000;23(10):985–95.
2. Vincent A, et al. Phenotypic characteristics including in vivo cone photoreceptor mosaic in KCNV2-related “cone dystrophy with supernormal rod electroretinogram”. Invest Ophthalmol Vis Sci. 2013;54(1):898–908.
3. Gundogan FC, Tas A, Sobaci G. Electroretinogram in hereditary retinal disorders. Electroretinograms. 2011;95–132.
4. Galli-Resta L, et al. Early detection of central visual function decline in cone-rod dystrophy by the use of macular focal cone electroretinogram. Invest Ophthalmol Vis Sci. 2013;54(10):6560–9.
5. Xiao X, et al. A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese family. Mol Vis. 2011;17:3271–8.