Severe Hyperinsulinaemic Hypoglycaemia in Beckwith-Wiedemann Syndrome due to Paternal Uniparental Disomy of 11p15.5 Managed with Sirolimus Therapy. (2016)
Attributed to:
Title: Understanding the molecular mechanisms of hyperinsulinaemic hypoglycaemia and developing novel therapies
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1159/000443398
PubMed Identifier: 26863215
Publication URI: http://europepmc.org/abstract/MED/26863215
Type: Journal Article/Review
Volume: 85
Parent Publication: Hormone research in paediatrics
Issue: 5
ISSN: 1663-2818