Publication | Open Access

A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly

Developmental AnomalyDevelopmental BiologyPeters AnomalyMendelian DisorderGenetic DisorderDevelopmental GeneticsGeneticsCraniofacial DevelopmentMorphogenesisMolecular GeneticsAutosomal Dominant FormDisease Gene IdentificationMedicineNon-stop Mutation