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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

dc.contributor.authorDe, Franco
dc.contributor.authorÖZCABı, Bahar
dc.contributor.authorErdoğan, H
dc.contributor.authorELLARD, S
dc.contributor.authorErcan, Oya
dc.contributor.authorEvliyaoğlu, O
dc.contributor.authorATAOĞLU, E
dc.contributor.authorZÜBARIOĞLU, Ü
dc.contributor.authorDağdeviren, A
dc.date.accessioned2021-03-02T23:13:25Z
dc.date.available2021-03-02T23:13:25Z
dc.identifier.citationEvliyaoğlu O., Ercan O., ATAOĞLU E., ZÜBARIOĞLU Ü., ÖZCABı B., Dağdeviren A., Erdoğan H., De F., ELLARD S., "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", Journal of clinical research in pediatric endocrinology, cilt.10, ss.168-174, 2018
dc.identifier.issn1308-5727
dc.identifier.othervv_1032021
dc.identifier.otherav_1130a25e-c46e-4218-a1ce-4f6a5acbddb3
dc.identifier.urihttp://hdl.handle.net/20.500.12627/17039
dc.identifier.urihttps://doi.org/10.4274/jcrpe.5162
dc.language.isoeng
dc.titleNeonatal 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
dc.typeMakale
dc.relation.journalJournal of clinical research in pediatric endocrinology
dc.contributor.department, ,
dc.identifier.volume10
dc.identifier.startpage168
dc.identifier.endpage174
dc.contributor.firstauthorID123488


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