Fig. 1From: A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutationClinical images and family pedigree of three families with isolated band keratopathy. a Pedigree of three families. Red arrows indicate the proband in each family. b Photograph of individual F1:V2 shows band keratopathy in both the right and left eyeBack to article page