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Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemia. (2018)

First Author: Laver TW

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

Volume: 89

Parent Publication: Clinical endocrinology

Issue: 5

ISSN: 0300-0664