An investigation into LOXL1 variants in black South African individuals with exfoliation syndrome.

doi:10.1001/archophthalmol.2010.349

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Article

An investigation into LOXL1 variants in black South African individuals with exfoliation syndrome.

Archives of ophthalmology (Chicago, Ill. : 1960) - 1 Feb 2011

Rautenbach Robyn M, Bardien Soraya, Harvey Justin, Ziskind Ari

Abstract excerpt

OBJECTIVE: To investigate the association between 2 lysyl oxidase-like 1 (LOXL1) polymorphisms, rs1048661 (R141L) and rs3825942 (G153D), and exfoliation syndrome (XFS) in black South African individuals. METHODS: A total of 43 black patients with XFS and 47 ethnically matched controls were recruited for genetic analysis. Samples were analyzed for presence of the LOXL1-R141L and G153D variants using restriction...

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Source

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Identifiers

PMID: 21320968
DOI: 10.1001/archophthalmol.2010.349

Genes

LOXL1

Variants

rs1048661
rs1048661

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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