O. Cohen

Four Novel Mutations, Including the First Gross Deletion in TCF1, identified in HNF4a, GCK and TCF1 in Patients with MODY in Israel

S. Shalitin, M. Phillip, R. Nimri, 2007, Journal of pediatric endocrinology & metabolism : JPEM.

Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity.

J. Beckmann, J. Weissenbach, D. Paslier, 1994, Genomics.

The glucokinase mutation p.T206P is common among MODY patients of Jewish Ashkenazi descent

T. Oron, S. Shalitin, M. Phillip, 2012, Pediatric diabetes.