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Clinical Characterization of LRPAP1-Related Pediatric High Myopia.
Khan AO, Aldahmesh MA, Alkuraya FS. Khan AO, et al. Among authors: aldahmesh ma. Ophthalmology. 2016 Feb;123(2):434-435. doi: 10.1016/j.ophtha.2015.06.051. Epub 2015 Aug 11. Ophthalmology. 2016. PMID: 26271838 No abstract available.
The distinct ophthalmic phenotype of Knobloch syndrome in children.
Khan AO, Aldahmesh MA, Mohamed JY, Al-Mesfer S, Alkuraya FS. Khan AO, et al. Among authors: aldahmesh ma. Br J Ophthalmol. 2012 Jun;96(6):890-5. doi: 10.1136/bjophthalmol-2011-301396. Epub 2012 Mar 7. Br J Ophthalmol. 2012. PMID: 22399687
Mutations in LRPAP1 are associated with severe myopia in humans.
Aldahmesh MA, Khan AO, Alkuraya H, Adly N, Anazi S, Al-Saleh AA, Mohamed JY, Hijazi H, Prabakaran S, Tacke M, Al-Khrashi A, Hashem M, Reinheckel T, Assiri A, Alkuraya FS. Aldahmesh MA, et al. Am J Hum Genet. 2013 Aug 8;93(2):313-20. doi: 10.1016/j.ajhg.2013.06.002. Epub 2013 Jul 3. Am J Hum Genet. 2013. PMID: 23830514 Free PMC article.
76 results