Open AccessCongenital Hyperinsulinism and Glucose Hypersensitivity in Homozygous and Heterozygous Carriers of Kir6.2 (KCNJ11) Mutation V290M Mutation: KATP Channel Inactivation Mechanism and Clinical Management
Author(s) -
K. J. Loechner,
A. Akrouh,
H. T. Kurata,
C. Dionisi-Vici,
A. Maiorana,
M. Pizzoferro,
V. Rufini,
Jean de Ville de Goyet,
C. Colombo,
F. Barbetti,
J. C. Koster,
C. G. Nichols
Publication year - 2011
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/kxzx-3q92
Subject(s) - kir6.2 , mutation , congenital hyperinsulinism , hyperinsulinism , mechanism (biology) , medicine , endocrinology , genetics , biology , protein subunit , insulin , gene , insulin resistance , epistemology , philosophy