Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?

Rozenkova, K; Nessa, A; Obermannova, B; Elblova, L; Dusatkova, P; Sumnik, Z; Lebl, J; Hussain, K; Pruhova, S

Dusatkova, P (reprint author), Charles Univ Prague, Univ Hosp Motol, Fac Med 2, Dept Pediat, V Uvalu 84, Prague 15006 5, Czech Republic.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2017; 30 (12): 1311

Abstract

Background: Congenital hyperinsulinism (CHI) is frequently caused by mutations in one of the K-ATP channel subunits encoded by the genes ABCC8 and KCN......

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