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Nanophthalmos: A Review of the Clinical Spectrum and Genetics.
Carricondo PC, Andrade T, Prasov L, Ayres BM, Moroi SE. Carricondo PC, et al. Among authors: moroi se. J Ophthalmol. 2018 May 9;2018:2735465. doi: 10.1155/2018/2735465. eCollection 2018. J Ophthalmol. 2018. PMID: 29862063 Free PMC article. Review.
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.
Garnai SJ, Brinkmeier ML, Emery B, Aleman TS, Pyle LC, Veleva-Rotse B, Sisk RA, Rozsa FW, Ozel AB, Li JZ, Moroi SE, Archer SM, Lin CM, Sheskey S, Wiinikka-Buesser L, Eadie J, Urquhart JE, Black GCM, Othman MI, Boehnke M, Sullivan SA, Skuta GL, Pawar HS, Katz AE, Huryn LA, Hufnagel RB; Genomic Ascertainment Cohort; Camper SA, Richards JE, Prasov L. Garnai SJ, et al. Among authors: moroi se. PLoS Genet. 2019 May 2;15(5):e1008130. doi: 10.1371/journal.pgen.1008130. eCollection 2019 May. PLoS Genet. 2019. PMID: 31048900 Free PMC article.
Glaucoma and Cornea Surgery Outcomes in Peters Anomaly.
Dolezal KA, Besirli CG, Mian SI, Sugar A, Moroi SE, Bohnsack BL. Dolezal KA, et al. Among authors: moroi se. Am J Ophthalmol. 2019 Dec;208:367-375. doi: 10.1016/j.ajo.2019.08.012. Epub 2019 Aug 28. Am J Ophthalmol. 2019. PMID: 31470000
127 results