Characterising PRPF31-associated retinal dystrophy : Clinical insights from baseline data in a natural history study
Purpose: To characterise the baseline clinical features and genotypes of adults with pre-mRNA processing factor 31 (PRPF31)-associated retinal dystrophy (RD) enrolled in a prospective, multicentre 4-year natural history study, and to explore correlations between selected baseline parameters. Methods: Thirty-one patients with PRPF31-RD underwent comprehensive multimodal assessment, including slit-l
