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

Yazar
De, Franco
ÖZCABı, Bahar
Erdoğan, H
ELLARD, S
Ercan, Oya
Evliyaoğlu, O
ATAOĞLU, E
ZÜBARIOĞLU, Ü
Dağdeviren, A
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http://hdl.handle.net/20.500.12627/17039
https://doi.org/10.4274/jcrpe.5162
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