GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Author:
Funder
Foundation for Polish Science
Publisher
Elsevier BV
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Reference88 articles.
1. Genetics of exfoliation syndrome and glaucoma;Aboobakar;Int. Ophthalmol. Clin.,2014
2. LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients;Álvarez;BMC Med. Genet.,2015
3. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci;Aung;Nat. Genet.,2017
4. A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome;Aung;Nat. Genet.,2015
5. Epidemiology of pseudoexfoliation syndrome: demystifying legends and looking to the future;Benitez-del-Castillo Sanchez;Arch. Soc. Esp. Oftalmol.,2015
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4. Role of clusterin gene 3’-UTR polymorphisms and promoter hypomethylation in the pathogenesis of pseudoexfoliation syndrome and pseudoexfoliation glaucoma;Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms;2023-12
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