Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations

OBJECTIVE: The phenotype associated with heterozygous HNF4A gene mutations has recently been extended to include diazoxide responsive neonatal hypoglycemia in addition to maturity-onset diabetes of the young (MODY). To date, mutation screening has been limited to patients with a family history consi...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Flanagan, S E, Kapoor, R R, Mali, G, Cody, D, Murphy, N, Schwahn, B, Siahanidou, T, Banerjee, I, Akcay, T, Rubio-Cabezas, O, Shield, J P H, Hussain, K, Ellard, S
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioScientifica 2010
Aiheet:
Clinical Study
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2857991/
https://ncbi.nlm.nih.gov/pubmed/20164212
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EJE-09-0861
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