Valleix, S., Niel, F., Nedelec, B., Algros, M., Schwartz, C., Delbosc, B., . . . Kantelip, B. (2006). Homozygous Nonsense Mutation in the FOXE3 Gene as a Cause of Congenital Primary Aphakia in Humans. The American Society of Human Genetics.

Valleix, Sophie, Florence Niel, Brigitte Nedelec, Marie-Paule Algros, Claire Schwartz, Bernard Delbosc, Marc Delpech, und Bernadette Kantelip. Homozygous Nonsense Mutation in the FOXE3 Gene As a Cause of Congenital Primary Aphakia in Humans. The American Society of Human Genetics, 2006.

Valleix, Sophie, et al. Homozygous Nonsense Mutation in the FOXE3 Gene As a Cause of Congenital Primary Aphakia in Humans. The American Society of Human Genetics, 2006.