Open AccessAssociation of LOXL1 gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Author(s) -
Wisam Shihadeh,
Omar F. Khabour,
Mohammed Khalil,
Alaa Al-Dabbagh,
Mustafa Al-Hashimi
Publication year - 2018
Publication title -
international journal of ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.634
H-Index - 29
eISSN - 2227-4898
pISSN - 2222-3959
DOI - 10.18240/ijo.2018.10.02
Subject(s) - single nucleotide polymorphism , snp , medicine , haplotype , genotype , allele , genetics , allele frequency , genotype frequency , glaucoma , genetic association , gene , ophthalmology , biology
To investigate the association between single nucleotide polymorphisms (SNPs) in the LOXL1 gene with exfoliation syndrome/glaucoma (XFS/XFG) among Jordanians.
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