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 İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 10
  • Basım Tarihi: 2018
  • Doi Numarası: 10.4274/jcrpe.5162
  • Dergi Adı: Journal of clinical research in pediatric endocrinology
  • Sayfa Sayıları: ss.168-174