LOXL3 and myopia: To date, 27 loci (MYP1-MYP28, MYP4 was deprived) and ten genes (OPN1LW, OMIM 300822; SCO2, OMIM 604272; ZNF644, OMIM 614159; CCDC111, OMIM 615421; LRPAP1, OMIM 104225; SLC39A5, OMIM 608730; P4HA2, OMIM 600608; ARR3, OMIM 301770, CPSF1, OMIM 606027; LOXL3, OMIM 607163) are identified to be associated with myopia by linkage analysis combined with whole-exome sequencing (WES) or WES alone, which account for less than 15% patients with eoHM [5,6].