The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy.

Sandal, T; Laborie, L B; Brusgaard, K; Eide, S A; Christesen, H B T; Søvik, O; Njølstad, P R; Molven, A

Sandal, T; Laborie, L B; Brusgaard, K; Eide, S A; Christesen, H B T; Søvik, O; Njølstad, P R; Molven, A.

Affiliation

Sandal T; aSection for Pathology, The Gade Institute, and bSection for Pediatrics, Department of Clinical Medicine, University of Bergen, Norway.

Clin Genet ; 75(5): 440-8, 2009 May.

Article in En | MEDLINE | ID: mdl-19475716

Subject(s)

ATP-Binding Cassette Transporters/genetics; Congenital Hyperinsulinism/genetics; Mutation; Potassium Channels, Inwardly Rectifying/genetics; Receptors, Drug/genetics; Cohort Studies; Female; Genetic Testing; Humans; Infant, Newborn; Male; Norway; Pedigree; Sulfonylurea Receptors

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Database: MEDLINE Main subject: Receptors, Drug / ATP-Binding Cassette Transporters / Potassium Channels, Inwardly Rectifying / Congenital Hyperinsulinism / Mutation Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Newborn Country/Region as subject: Europa Language: En Year: 2009 Type: Article

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