Congenital Hyperinsulinism and Glucose Hypersensitivity in Homozygous and Heterozygous Carriers of Kir6.2 (KCNJ11) Mutation V290M Mutation: KATP Channel Inactivation Mechanism and Clinical Management

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Title
Congenital Hyperinsulinism and Glucose Hypersensitivity in Homozygous and Heterozygous Carriers of Kir6.2 (KCNJ11) Mutation V290M Mutation: KATP Channel Inactivation Mechanism and Clinical Management
Authors
Keywords
-
Journal
DIABETES
Volume 60, Issue 1, Pages 209-217
Publisher
American Diabetes Association
Online
2010-10-28
DOI
10.2337/db10-0731

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