Associated Papers
Genetics of Keratoconus: A Comprehensive Review.
Barcelo-Canton RH et al.
Genes, 2025
Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy.
Liu S et al.
Acta Ophthalmologica, 2023
Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the Literature.
Zhu D et al.
International Journal of Molecular Sciences, 2023
36902444 (PubMed )
Supplement: ijms-24-05012-s001.zip › ijms-2152855-Supplementary_Table_S4_.xlsx › Sheet1
Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs' endothelial corneal dystrophy.
Tsedilina TR et al.
Frontiers in Medicine, 2023
37441688 (PubMed )
Supplement: Table_1.xlsx › ZEB1_cases
Genetic Screening Revealed Latent Keratoconus in Asymptomatic Individuals.
Chen S et al.
Frontiers in Cell and Developmental Biology, 2021
Genetics in Keratoconus: where are we?
Bykhovskaya Y et al.
Eye and Vision (london, England), 2016
First identification of a triple corneal dystrophy association: keratoconus, epithelial basement membrane corneal dystrophy and fuchs' endothelial corneal dystrophy.
Mazzotta C et al.
Case Reports in Ophthalmology, 2014
Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.
Lechner J et al.
Investigative Ophthalmology & Visual Science, 2013
Select a paper to view details