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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)

First Author: Demirbilek H

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