Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations. (2015)
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/10.1530/eje-14-0852
PubMed Identifier: 25755231
Publication URI: http://europepmc.org/abstract/MED/25755231
Type: Journal Article/Review
Volume: 172
Parent Publication: European journal of endocrinology
Issue: 6
ISSN: 0804-4643