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Article

Analysis of LOXL1 single nucleotide polymorphisms in Polish population with pseudoexfoliation syndrome.

Acta ophthalmologica - 1 Feb 2011

Malukiewicz Grażyna, Lesiewska-Junk Hanna, Linkowska Katarzyna, Mielnik Marta, Grzybowski Tomasz, Sulima Natalia

Abstract excerpt

PURPOSE: To assess the possible association of lysyl oxidase-like 1 (LOXL1) gene variants with pseudoexfoliation syndrome (PEX) in Polish population. METHODS: The group studied comprised of 36 patients with PEX (men and women) who presented to Department of Ophthalmology Collegium Medicum UMK in Bydgoszcz, Poland, and 30 control subjects. Blood samples were obtained from each patient via peripheral venipuncture,...

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Source

Identifiers

PMID: 21272281
DOI: 10.1111/j.1755-3768.2010.02083.x

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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