Koufakis, T., Sertedaki, A., Tatsi, E., Trakatelli, C., Karras, S. N., Manthou, E., . . . Kotsa, K. (2019). First Report of Diabetes Phenotype due to a Loss-of-Function ABCC8 Mutation Previously Known to Cause Congenital Hyperinsulinism. Case Rep Genet.

Koufakis, Theocharis, Amalia Sertedaki, Elizabeth-Barbara Tatsi, Christina-Maria Trakatelli, Spyridon N. Karras, Eleni Manthou, Christina Kanaka-Gantenbein, und Kalliopi Kotsa. "First Report of Diabetes Phenotype Due to a Loss-of-Function ABCC8 Mutation Previously Known to Cause Congenital Hyperinsulinism." Case Rep Genet 2019.

Koufakis, Theocharis, et al. "First Report of Diabetes Phenotype Due to a Loss-of-Function ABCC8 Mutation Previously Known to Cause Congenital Hyperinsulinism." Case Rep Genet 2019.