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Article

Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus.

Cornea - 1 Feb 2010

Stabuc-Silih Mirna, Strazisar Mojca, Hawlina Marko, Glavac Damjan

Abstract excerpt

PURPOSE: Keratoconus (KC) is a bilateral, noninflammatory, and progressive corneal ectasia that occurs mostly as a sporadic disorder, but it has long been recognized that a significant minority of patients also exhibit a family history. In recent years, several candidate genes, including VSX1 and...

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Source

Identifiers

PMID: 20023586
DOI: 10.1097/ICO.0b013e3181aebf7a

Genes

VSX1
SOD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20023586-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus.PMID 20023586Read ↗

Genetics and clinical characteristics of keratoconus.Semantic proximity Read ↗

Absence of significant genetic alterations in the VSX1, SOD1, TIMP3, and LOX genes in Brazilian patients with Keratoconus.Semantic proximity Read ↗

Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.Semantic proximity Read ↗

Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus.Semantic proximity Read ↗

Polymorphism Analysis of VSX1 and SOD1 Genes in Greek Patients with Keratoconus.Semantic proximity Read ↗

Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus.Semantic proximity Read ↗

Analysis of the VSX1 gene in sporadic keratoconus patients from China.Semantic proximity Read ↗

Mutational screening of VSX1 in keratoconus patients from the European population.Semantic proximity Read ↗

No VSX1 gene mutations associated with keratoconus.Semantic proximity Read ↗

[A novel VSX1 gene mutation identified in a sporadic keratoconus patient from China].Semantic proximity Read ↗

Molecular analysis of the VSX1 gene in familial keratoconus.Semantic proximity Read ↗

VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation.Semantic proximity Read ↗

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