Nicolino, M., Claiborn, K. C., Senée, V., Boland, A., Stoffers, D. A., & Julier, C. (2010). A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency. American Diabetes Association.

Nicolino, Marc, Kathryn C. Claiborn, Valérie Senée, Anne Boland, Doris A. Stoffers, and Cécile Julier. A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency. American Diabetes Association, 2010.

Nicolino, Marc, et al. A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency. American Diabetes Association, 2010.