Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.

Permanent neonatal diabetes (PND) can be caused by mutations in the transcription factors insulin promoter factor (IPF)-1, eukaryotic translation initiation factor-2alpha kinase 3 (EIF2AK3), and forkhead box-P3 and in key components of insulin secretion: glucokinase (GCK) and the ATP-sensitive K(+)...

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Detalles Bibliográficos
Main Authors:	Sagen, J, Raeder, H, Hathout, E, Shehadeh, N, Gudmundsson, K, Baevre, H, Abuelo, D, Phornphutkul, C, Molnes, J, Bell, G, Gloyn, A, Hattersley, A, Molven, A, Søvik, O, Njølstad, P
Formato:	Journal article
Idioma:	English
Publicado:	2004

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.

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