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