Associated Papers
Unilateral posterior polymorphous corneal dystrophy due to a novel ZEB1 gene mutation in a Korean girl.
Lee CY et al.
Ophthalmic Genetics, 2022
Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles.
Dudakova L et al.
Genes, 2021
Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation.
Nguyen DQ et al.
Acta Ophthalmologica, 2010
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