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Article

Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.

BMC research notes - 18 Mar 2013

Verma Anshuman, Das Manoranjan, Srinivasan Muthiah, Prajna Namperumalsamy V, Sundaresan Periasamy

Abstract excerpt

BACKGROUND: The involvement of VSX1 gene for the genetic basis of keratoconus is unclear and controversial. The genetic screening of VSX1 from different ethnic populations can enlighten this subject. The aim of the present study is to investigate the role of VSX1 gene in patients with sporadic cases of keratoconus from South India. METHODS: The VSX1 gene coding regions, including exon-intron boundaries were...

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Identifiers

PMID: 23506487
DOI: 10.1186/1756-0500-6-103
PMCID: PMC3608990

Genes

VSX1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.PMID 23506487Read ↗

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

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