ArticleJournal of clinical research in pediatric endocrinology2018

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

Olcay Evliyaoğlu et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.