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Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation. (2019)

First Author: Isik E

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/10.4274/jcrpe.galenos.2018.2018.0077

PubMed Identifier: 29739729

Publication URI: http://europepmc.org/abstract/MED/29739729

Type: Journal Article/Review

Volume: 11

Parent Publication: Journal of clinical research in pediatric endocrinology

Issue: 1