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Article

Association of LOXL1 gene polymorphisms with exfoliation syndrome/glaucoma and primary open angle glaucoma in a Turkish population.

Molecular vision - 1 Jan 2013

Kasım Burcu, İrkeç Murat, Alikaşifoğlu Mehmet, Orhan Mehmet, Mocan Mehmet Cem, Aktaş Dilek

Abstract excerpt

PURPOSE: To investigate the association of lysyl oxidase like 1 (LOXL1) variants with exfoliation syndrome (XFS), exfoliation glaucoma (XFG), and primary open angle glaucoma (POAG) in a Turkish population. METHODS: Two LOXL1 single nucleotide polymorphisms (SNPs), rs1048661 (R141L) and rs3825942 (G153D), were analyzed in 300 Turkish patients (100 patients with XFS, 100 patients with XFG, 100 patients with POAG)...

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Source

Open in PubMed Open full text

Identifiers

PMID: 23378724
PMCID: PMC3559092

Genes

LOXL1

Variants

rs1048661
rs1048661

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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