Sulfonylurea Therapy in Two Korean Patients with Insulin-treated Neonatal Diabetes due to Heterozygous Mutations of the KCNJ11 Gene Encoding Kir6.2

Permanent neonatal diabetes (PND) is a rare form of diabetes characterized by insulin-requiring hyperglycemia diagnosed within the first three months of life. In most cases, the causes are not known. Recently, mutations in the KCNJ11 gene encoding the Kir6.2 subunit of the ATP-sensitive K(+) channel...

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Detalles Bibliográficos
Autores principales: Kim, Min Sun, Kim, Sun-Young, Kim, Gu-Hwan, Yoo, Han Wook, Lee, Dong Whan, Lee, Dae-Yeol
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2007
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693808/
https://www.ncbi.nlm.nih.gov/pubmed/17728498
http://dx.doi.org/10.3346/jkms.2007.22.4.616

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693808/
https://www.ncbi.nlm.nih.gov/pubmed/17728498
http://dx.doi.org/10.3346/jkms.2007.22.4.616

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