Abstract Objective Polymorphism rs13334190 in the zinc finger protein 469 gene has been suggested to predispose toward a “thin” cornea, which then becomes keratoconic or is directly pathogenic. Thus, we genotyped polymorphism rs13334190 in 127 unrelated keratoconus cases and 168 control subjects from Saudi Arabia using Taq-Man® assay. Results The genotype frequency distribution did not deviate significantly from the Hardy–Weinberg equilibrium (p > 0.05). Overall, both the genotype and allele frequencies were not significantly different between cases and controls. A minor allele frequency of 0.068 was comparable to the aggregate rates ranging from 0.060 to 0.086 observed in other populations. Binary logistic regression analysis was performed...
Keratoconus, a common inherited ocular disorder resulting in progressive corneal thinning, is the le...
Keratoconus (KC) is a degenerative corneal disorder for which the exact pathogenesis is not yet know...
Keratoconus is a bilateral, progressive corneal disease affecting all ethnic groups around the world...
PURPOSE. The Zinc Finger Protein 469 (ZNF469) gene has been proposed as a candidate gene for keratoc...
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 Internati...
Keratoconus is a bilateral, progressive corneal thinning disorder that is the leading indication for...
Purpose: Keratoconus (KC) is the most common primary ectatic corneal disease, characterized by progr...
Keratoconus is a relatively frequent disease leading to severe visual impairment. Existing therapies...
<div><p>Introduction</p><p>Keratoconus is a relatively frequent disease leading to severe visual imp...
Genetic associations for keratoconus could be useful for understanding disease pathogenesis and disc...
Many genes have been suggested as candidate genes for keratoconus based on their function, their pro...
Abstract Background Keratoconus is a chronic degenerative disorder of the cornea characterized by th...
Keratoconus, a common inherited ocular disorder resulting in progressive corneal thinning, is the le...
Many genes have been suggested as candidate genes for keratoconus based on their function, their pro...
Importance: Keratoconus is a condition in which the cornea progressively thins and protrudes in a co...
Keratoconus, a common inherited ocular disorder resulting in progressive corneal thinning, is the le...
Keratoconus (KC) is a degenerative corneal disorder for which the exact pathogenesis is not yet know...
Keratoconus is a bilateral, progressive corneal disease affecting all ethnic groups around the world...
PURPOSE. The Zinc Finger Protein 469 (ZNF469) gene has been proposed as a candidate gene for keratoc...
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 Internati...
Keratoconus is a bilateral, progressive corneal thinning disorder that is the leading indication for...
Purpose: Keratoconus (KC) is the most common primary ectatic corneal disease, characterized by progr...
Keratoconus is a relatively frequent disease leading to severe visual impairment. Existing therapies...
<div><p>Introduction</p><p>Keratoconus is a relatively frequent disease leading to severe visual imp...
Genetic associations for keratoconus could be useful for understanding disease pathogenesis and disc...
Many genes have been suggested as candidate genes for keratoconus based on their function, their pro...
Abstract Background Keratoconus is a chronic degenerative disorder of the cornea characterized by th...
Keratoconus, a common inherited ocular disorder resulting in progressive corneal thinning, is the le...
Many genes have been suggested as candidate genes for keratoconus based on their function, their pro...
Importance: Keratoconus is a condition in which the cornea progressively thins and protrudes in a co...
Keratoconus, a common inherited ocular disorder resulting in progressive corneal thinning, is the le...
Keratoconus (KC) is a degenerative corneal disorder for which the exact pathogenesis is not yet know...
Keratoconus is a bilateral, progressive corneal disease affecting all ethnic groups around the world...