Associated Papers
Ovol2 promoter mutations in mice and human illuminate species-specific phenotypic divergence.
Sunny SS et al.
Human Molecular Genetics, 2024
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
Update on the genetics of corneal endothelial dystrophies.
Kannabiran C et al.
Indian Journal of Ophthalmology, 2022
c.-61G>A in OVOL2 is a Pathogenic 5' Untranslated Region Variant Causing Posterior Polymorphous Corneal Dystrophy 1.
Janeschitz-Kriegl L et al.
Cornea, 2022
Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort.
Moon D et al.
Genes, 2021
35052368 (PubMed )
Supplement: genes-13-00027-s001.zip › genes-1495226-supplementary.pdf
Altered TERT promoter and other genomic regulatory elements: occurrence and impact.
Heidenreich B et al.
International Journal of Cancer, 2017
Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1.
Chung DD et al.
Plos One, 2017
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2.
Davidson AE et al.
American Journal of Human Genetics, 2016
Molecular genetics of cataract.
Kannabiran C et al.
Indian Journal of Ophthalmology, 2000
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