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


Evliyaoğlu O., Ercan O., ATAOĞLU E., ZÜBARIOĞLU Ü., ÖZCABı B., Dağdeviren A., ...Daha Fazla

Journal of clinical research in pediatric endocrinology, cilt.10, ss.168-174, 2018 (SCI-Expanded) identifier identifier identifier