Associated Papers
Genetics of Keratoconus: A Comprehensive Review.
Barcelo-Canton RH et al.
Genes, 2025
The association between VSX1 exon3 gene variants and keratoconus in Malaysian patients.
Deva JP et al.
Indian Journal of Ophthalmology, 2023
A comprehensive molecular genetic analysis of keratoconus patients from assam, a northeastern state of India.
Chakravarty M et al.
European Journal of Ophthalmology, 2022
rs12480307 and rs6050307 Polymorphisms of VSX1 Gene in Patient with Keratoconusin Southwest Iran Using PCR-RFLP.
Karami Eshkaftaki R et al.
Iranian Journal of Public Health, 2018
Novel visual system homeobox 1 gene mutations in Turkish patients with keratoconus.
Bardak H et al.
Genetics and Molecular Research : Gmr, 2016
Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification.
Karolak JA et al.
Ophthalmic Genetics, 2016
Two novel missense substitutions in the VSX1 gene: clinical and genetic analysis of families with Keratoconus from India.
Shetty R et al.
Bmc Medical Genetics, 2015
Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.
Verma A et al.
Bmc Research Notes, 2013
Study of VSX1 mutations in patients with keratoconus in southwest Iran using PCR-single-strand conformation polymorphism/heteroduplex analysis and sequencing method.
Dehkordi FA et al.
Acta Cytologica, 2013
VSX1 gene and keratoconus: genetic analysis in Korean patients.
Jeoung JW et al.
Cornea, 2012
Mutational screening of VSX1 in keratoconus patients from the European population.
Dash DP et al.
Eye (london, England), 2010
Molecular analysis of the VSX1 gene in familial keratoconus.
Liskova P et al.
Molecular Vision, 2007
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