Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype
Keywords: آموزش مداوم; CME; cystoid macular edema; ERG; electroretinogram; FAF; fundus autofluorescence; LCA; Leber congenital amaurosis; MP-1; microperimetry 1; MUPP1; multi-PDZ domain protein-1; RP; retinitis pigmentosa; RPE; retinal pigment epithelium; SD-OCT; spectral-domai