Verdin, H., Sorokina, E. A., Meire, F., Casteels, I., de Ravel, T., Semina, E. V., & De Baere, E. (2014). Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics. BioMed Central.

Verdin, Hannah, Elena A. Sorokina, Françoise Meire, Ingele Casteels, Thomy de Ravel, Elena V. Semina, e Elfride De Baere. Novel and Recurrent PITX3 Mutations in Belgian Families With Autosomal Dominant Congenital Cataract and Anterior Segment Dysgenesis Have Similar Phenotypic and Functional Characteristics. BioMed Central, 2014.

Verdin, Hannah, et al. Novel and Recurrent PITX3 Mutations in Belgian Families With Autosomal Dominant Congenital Cataract and Anterior Segment Dysgenesis Have Similar Phenotypic and Functional Characteristics. BioMed Central, 2014.