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Article

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

[Zhonghua yan ke za zhi] Chinese journal of ophthalmology - 11 Mar 2018

Guan T, Wu H J, Zhang L J, Xu D J, Zheng L B, Yao Y F

Abstract excerpt

Objective: To investigate the possibility of the visual system homeobox 1 (VSX1) gene as a candidate susceptibility gene for Chinese patients with sporadic keratoconus, and to identify sequence variants of the VSX1 gene in such patients. Methods: Cross-sectional study. Genomic DNA was extracted from the leukocytes in the peripheral venous blood of 50 patients with sporadic keratoconus and 50 control subjects...

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Identifiers

PMID: 29518881
DOI: 10.3760/cma.j.issn.0412-4081.2018.03.012

Genes

VSX1

Variants

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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.

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