Condition: Rare isolated myopia
rs773243225
in
LRPAP1
gene and
Rare isolated myopia
PMID 26271838
2016 Clinical Characterization of LRPAP1-Related Pediatric High Myopia.
PMID 25525168
2014 Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing.
PMID 23830514
2013 Mutations in LRPAP1 are associated with severe myopia in humans.