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Article

A novel VSX1 mutation identified in an individual with keratoconus in India.

Molecular vision - 28 Nov 2009

Paliwal Preeti, Singh Anuradha, Tandon Radhika, Titiyal Jeevan S, Sharma Arundhati

Abstract excerpt

PURPOSE: To evaluate the possible role of the VSX1 gene in a group of patients from the Indian subcontinent with keratoconus. METHODS: Molecular analysis of 66 patients with a diagnosis of keratoconus, based on clinical examination and corneal topography, was carried out. DNA extraction from peri...

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Source

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Identifiers

PMID: 19956409
PMCID: PMC2786886

Genes

VSX1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19956409-2026-09-02.2. 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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A novel VSX1 mutation identified in an individual with keratoconus in India.PMID 19956409Read ↗

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

Analysis of the VSX1 gene in keratoconus patients from Saudi Arabia.Semantic proximity Read ↗

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

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

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

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

VSX1 gene analysis in keratoconus.Semantic proximity Read ↗

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

Study of VSX1 mutations in patients with keratoconus in southwest Iran using PCR-single-strand conformation polymorphism/heteroduplex analysis and sequencing method.Semantic proximity Read ↗

VSX1 gene variants are associated with keratoconus in unrelated Korean patients.Semantic proximity Read ↗

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

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