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Congenital hyperinsulinism caused by hexokinase I expression or glucokinase-activating mutation in a subset of β-cells.
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Document type | Article de périodique (Journal article) – Article de recherche |
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Access type | Accès restreint |
Publication date | 2013 |
Language | Anglais |
Journal information | "Diabetes" - Vol. 62, no.5, p. 1689-1696 (2013) |
Peer reviewed | yes |
Publisher | American Diabetes Association ((United States) [S.l.]) |
issn | 0012-1797 |
e-issn | 1939-327X |
Publication status | Publié |
Affiliations |
UCL
- SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition UCL - SSS/IREC/GAEN - Pôle d'Hépato-gastro-entérologie UCL - (SLuc) Service d'anatomie pathologique |
MESH Subject | Amino Acid Substitution ; Insulin-Secreting Cells ; Mutation ; Tolbutamide ; Diazoxide ; Glucokinase ; Hexokinase ; Humans ; Hyperinsulinism ; Hypoglycemic Agents ; Infant, Newborn ; Insulin |
Links |
Bibliographic reference | Henquin, Jean-Claude ; Sempoux, Christine ; Marchandise, Joelle ; Godecharles, Sebastien ; Guiot, Yves ; et. al. Congenital hyperinsulinism caused by hexokinase I expression or glucokinase-activating mutation in a subset of β-cells.. In: Diabetes, Vol. 62, no.5, p. 1689-1696 (2013) |
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Permanent URL | http://hdl.handle.net/2078.1/136278 |