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Successful sulfonylurea treatment in a patient with permanent neonatal diabetes mellitus with a novel KCNJ11 mutation

Sung Yeon Ahn, Gu-Hwan Kim, Han-Wook Yoo

Clin Exp Pediatr. 2015;58(8):309-312. Published online August 21, 2015

Permanent neonatal diabetes mellitus refers to diabetes that occurs before the age of 6 months and persists through life. It is a rare disorder affecting one in 0.2-0.5 million live births. Mutations in the gene KCNJ11, encoding the subunit Kir6.2, and ABCC8, encoding SUR1 of the ATP-sensitive potassium (K_ATP) channel, are the most common causes of permanent neonatal diabetes mellitus....

DOI: https://doi.org/10.3345/kjp.2015.58.8.309

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