9Chograni M, Alkuraya F, Ourteni I, Maazoul F, Lariani I, Chaabouni HB. Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family. Clin Genet. 2014 Oct 30. doi: 10. 1111/cge. 12489. [ Epub ahead of print] PubMed PMID: 25358429.
10Chert JH, Qiu J, Chen H, Pang CP, Zhang M. Rapid and cost - effective molecular diagnosis using exome sequencing of one proband with autosomal dominant congenital cataract. Eye (Lond). 2014 Oct 10. doi: 10. 1038/eye. 2014. 158. [ Epub ahead of print] PubMed PMID: 25301372.