LRPAP1

Publications

Aldahmesh MA et al. Mutations in LRPAP1 are associated with severe myopia in humans. Am J Hum Genet. 2013;93(2):313-20.  PMID: 23830514.

Khan AO et al. Clinical characterization of LRPAP1-related pediatric high myopia. Ophthalmology. 2016;123(2):434-5.  PMID: 26271838.

Jiang D et al. Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing. Invest Ophthalmol Vis Sci. 2014;56(1):339-45.  PMID: 25525168.

Feng CY et al. Mutational screening of SLC39A5, LEPREL1 and LRPAP1 in a cohort of 187 high myopia patients. Sci Rep. 2017;7(1):1120.  PMID:28442722.