NR2E3 and Goldmann-Favre syndrome: The missense mutation c.925C > T of NR2E3 is a novel mutation for Goldmann-Favre syndrome, but the c.925C > G (p.R309G) at the same location of mRNA and polypeptide chain is known to be pathogenic for Goldmann-Favre syndrome and enhanced S-cone syndrome [16].