Evliyaoğlu, O., Ercan, O., Ataloğlu, E., Zübarioğlu, Ü., Özcabı, B., Dağdeviren, A., . . . Ellard, S. (2018). Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation. J Clin Res Pediatr Endocrinol.
Citación estilo ChicagoEvliyaoğlu, Olcay, Oya Ercan, Emel Ataloğlu, Ümit Zübarioğlu, Bahar Özcabı, Aydilek Dağdeviren, Hande Erdoğan, Elisa De Franco, and Sian Ellard. "Neonatal Diabetes: Two Cases With Isolated Pancreas Agenesis Due to Homozygous PTF1A Enhancer Mutations and One With Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome Due to KCNJ11 Mutation." J Clin Res Pediatr Endocrinol 2018.
Cita MLAEvliyaoğlu, Olcay, et al. "Neonatal Diabetes: Two Cases With Isolated Pancreas Agenesis Due to Homozygous PTF1A Enhancer Mutations and One With Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome Due to KCNJ11 Mutation." J Clin Res Pediatr Endocrinol 2018.