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Article

Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.

Investigative ophthalmology & visual science - 1 Apr 2008

Pasutto Francesca, Krumbiegel Mandy, Mardin Christian Y, Paoli Daniela, Lämmer Robert, Weber Bernhard H F, Kruse Friedrich E, Schlötzer-Schrehardt Ursula, Reis André

Abstract excerpt

PURPOSE: Three common sequence variants in the lysyl oxidase-like 1 (LOXL1) gene were recently associated with both pseudoexfoliation (PEX) and pseudoexfoliation glaucoma (PEXG) in populations from Iceland and Sweden. In this study, the genetic association of these variants was investigated in patients with PEX or PEXG of German and Italian descent. METHODS: The three LOXL1 single-nucleotide polymorphisms (SNPs),...

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Source

Identifiers

PMID: 18385063
DOI: 10.1167/iovs.07-1449

Genes

LOXL1

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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