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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 peripheral blood followed by Polymerase Chain Reaction (PCR) amplification of the VSX1 gene was performed. The entire...

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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 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 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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