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Severe Hyperinsulinaemic Hypoglycaemia in Beckwith-Wiedemann Syndrome due to Paternal Uniparental Disomy of 11p15.5 Managed with Sirolimus Therapy. (2016)

First Author: Güemes M

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