Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemia (2018)
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/10.1111/cen.13841
PubMed Identifier: 30238501
Publication URI: http://europepmc.org/abstract/MED/30238501
Type: Journal Article/Review
Parent Publication: Clinical Endocrinology
Issue: 5
ISSN: 0300-0664