A syndrome of congenital hyperinsulinism and rhabdomyolysis is caused byKCNJ11mutation
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Reference21 articles.
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3. Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor;Dunne;N Engl J Med,1997
4. Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy;Thomas;Hum Mol Genet,1996
5. Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes;Gloyn;N Engl J Med,2004
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