Mutations in RLBP1 cause a range of retinopathies including retinitis punctata albescens (RPA), Bothnia‐type dystrophy (BD), Newfoundland rod‐cone dystrophy (NFRCD), RP and fundus albipunctatus (FA).69 This evidence concerns the gene RLBP1 and Newfoundland cone-rod dystrophy.