Skip to search formSkip to main contentSkip to account menu

ZNF469 gene

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

Related topics

Related topics

1 relation
Zinc Fingers

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
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… 
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… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)