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Article

Exploring functional candidate genes for genetic association in german patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.

Investigative ophthalmology & visual science - 1 Jun 2009

Krumbiegel Mandy, Pasutto Francesca, Mardin Christian Y, Weisschuh Nicole, Paoli Daniela, Gramer Eugen, Zenkel Matthias, Weber Bernhard H F, Kruse Friedrich E, Schlötzer-Schrehardt Ursula, Reis André

Abstract excerpt

PURPOSE: Pseudoexfoliation (PEX) syndrome is a generalized elastic microfibrillopathy characterized by fibrillar deposits in intra- and extraocular tissues. Genetic and nongenetic factors are known to be involved in its etiopathogenesis. This study was focused on six functional candidate genes in...

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Source

Identifiers

PMID: 19182256
DOI: 10.1167/iovs.08-2339

Genes

CLU
FBN1
LTBP2
MFAP2
TGM2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19182256-2026-09-04.1. Manifest publication-graph-cohort-2026-09-04.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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