LOXL1 gene analysis in Turkish patients with exfoliation glaucoma
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://link.springer.com/content/pdf/10.1007/s10792-016-0174-y.pdf
Reference27 articles.
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2. Ritch R, Schlötzer-Schrehardt U, Konstas AG (2003) Why is glaucoma associated with exfoliation syndrome? Prog Retin Eye Res 22(3):253–275
3. Damji KF, Bains HS, Stefansson E et al (1998) Is pseudoexfoliation syndrome inherited? A review of genetic and nongenetic factors and a new observation. Ophthalmic Genet 19(4):175–185
4. Orr AC, Robitaille JM, Price PA et al (2001) Exfoliation syndrome: clinical and genetic features. Ophthalmic Genet 22(3):171–185
5. Allingham RR, Loftsdottir M, Gottfredsdottir MS et al (2001) Pseudoexfoliation syndrome in Icelandic families. Br J Ophthalmol 85(6):702–707
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3. Single nucleotide polymorphisms in LOXL1 as biomarkers for progression of exfoliation glaucoma in Sweden;Acta Ophthalmologica;2022-12-23
4. Unexpected findings: Loss of Corneal Endothelial Cells in Uygur Patients with Exfoliation syndrome in XinJiang, China;2022-12-14
5. DNA Polymorphism of the LOXL1 Promoter Region in Exfoliation Syndrome in Uygur Individuals in XinJiang, China;Journal of Ophthalmology;2022-07-30
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