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ZNF469 gene

Known as: KIAA1858, ZINC FINGER PROTEIN 469, ZNF469 
National Institutes of Health

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Zinc Fingers

Papers overview

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2019
2019
Corneal Perforation After Corneal Cross-Linking in Keratoconus Associated With Potentially Pathogenic ZNF469 Mutations.
PURPOSE To report a case of bilateral and repetitive corneal perforations after corneal cross-linking (CXL) for keratoconus in a… 
2019
2019
Contributions of the superoxide dismutase 1 and zinc finger protein 469 (ZNF469) genes to keratoconus.
Keratoconus (KC) is a multifactorial, progressive, degenerative corneal disorder with an incidence of approximately 1 in 2,000… 
2017
2017
Novel Zinc Finger Protein Gene 469 (ZNF469) Variants in Advanced Keratoconus
ABSTRACT Purpose: Common polymorphic variants upstream of Zinc finger protein gene 469 (ZNF469) have been associated with central… 
2017
2017
Polymorphism rs13334190 in zinc finger protein 469 (ZNF469) is not a risk factor for keratoconus in a Saudi cohort
Polymorphism rs13334190 in the zinc finger protein 469 gene has been suggested to predispose toward a “thin” cornea, which then… 
2016
2016
Evidence against ZNF469 being causative for keratoconus in Polish patients
Keratoconus (KTCN) is a degenerative disorder characterized by stromal thinning and protrusion of the cornea, resulting in severe… 
2016
2016
Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue
Ehlers–Danlos syndrome (EDS) describes a group of clinical entities in which the connective tissue, primarily that of the skin… 
2012
2012
Brittle cornea without clinically-evident extraocular findings in an adult harboring a novel homozygous ZNF469 mutation
Recessive mutations in zinc finger protein 469 (ZNF469) cause the brittle cornea syndrome (Mendelian Inheritance in Man #229200… 
2012
2012
The Brittle Cornea Syndrome: Study of a family with five affected siblings
Purpose To define the natural history,genotype‐phenotype correlation and differential diagnosis of the Brittle Cornea Syndrome… 
2011
2011
Mutations in PRDM5 and ZNF469 cause brittle cornea syndrome by influencing extracellular matrix development and maintenance
Extreme corneal fragility and thinning, with a high risk of catastrophic spontaneous rupture, is the most devastating feature of… 
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