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Article

Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus.

Molecular vision - 15 Feb 2011

Paliwal Preeti, Tandon Radhika, Dube Divya, Kaur Punit, Sharma Arundhati

Abstract excerpt

PURPOSE: To look for segregation of Visual System Homeobox 1 (VSX1) mutations in family members of a patient with keratoconus. METHODS: Our initial molecular genetic studies conducted to identify the role of VSX1 in the causation of keratoconus had identified a novel mutation in one patient. He l...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 21365019
PMCID: PMC3042359

Genes

VSX1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21365019-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus.PMID 21365019Read ↗

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

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