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

K. J. Loechner, A. Akrouh, H. T. Kurata, C. Dionisi-Vici, A. Maiorana, M. Pizzoferro, V. Rufini, J. de Ville de Goyet, C. Colombo, F. Barbetti, J. C. Koster, C. G. Nichols
  • Diabetes, October 2010, American Diabetes Association
  • DOI: 10.2337/db10-0731

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The following have contributed to this page: Professor Jean de VILLE de GOYET