AIPL1 and Leber congenital amaurosis: Repair of AIPL1 c.665G>A, p.Trp222∗ in the compound heterozygous LCA patient iPSC line was achieved using ABE with ABEmax-VRQR and AIPL1 c.665G>A-A6-sgRNA, while a CRISPR-Cas9-HDR strategy was used to knock in (KI) c.665G>A, p.Trp222∗ (Figure S4; Table S4).