Associated Papers
Loss-of-function variants in ZEB1 cause dominant anomalies of the corpus callosum with favourable cognitive prognosis.
Heide S et al.
Journal of Medical Genetics, 2024
Posterior Polymorphous Corneal Dystrophy in a Patient with a Novel ZEB1 Gene Mutation.
Fernández-Gutiérrez E et al.
International Journal of Molecular Sciences, 2022
Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.
Lechner J et al.
Investigative Ophthalmology & Visual Science, 2013
Select a paper to view details