Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clinical heterogeneity of abnormal glucose homeostasis associated with the HNF4A R311H mutation.

Italian journal of pediatrics - 19 Jun 2014

Delvecchio Maurizio, Di Paola Rosa, Mangiacotti Davide, Sacco Michele, Menzaghi Claudia, Trischitta Vincenzo

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Blood Glucose
Share to Child
Share to Diabetes Mellitus, Type 2
Share to Exons

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hepatocyte Nuclear Factor 4

Share to Homeostasis

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 24947580
DOI: 10.1186/1824-7288-40-58
PMCID: PMC4100025

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical heterogeneity of abnormal glucose homeostasis associated with the HNF4A R311H mutation.PMID 24947580Read ↗

Mutation in the HNF-4alpha gene affects insulin secretion and triglyceride metabolism.Semantic proximity Read ↗

Clinical heterogeneity of hyperinsulinism due to HNF1A and HNF4A mutations.Semantic proximity Read ↗

HNF4A genetic variants: role in diabetes.Semantic proximity Read ↗

A role for coding functional variants in HNF4A in type 2 diabetes susceptibility.Semantic proximity Read ↗

The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes.Semantic proximity Read ↗

Genetic and clinical characteristics of patients with HNF1A gene variations from the German-Austrian DPV database.Semantic proximity Read ↗

Human gain-of-function variants in HNF1A confer protection from diabetes but independently increase hepatic secretion of multiple cardiovascular disease risk factorsSemantic proximity Read ↗

[HNF-1alpha G319S mutation in Oji-Cree type 2 diabetes].Semantic proximity Read ↗

Macrosomia, transient neonatal hypoglycemia, and monogenic diabetes in a family with heterozygous mutation R154X of HNF4A gene.Semantic proximity Read ↗

FNIP1 variants are associated with favourable metabolism in 1 million humansSemantic proximity Read ↗

Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4alpha mutations in a large European collection.Semantic proximity Read ↗

HNF4α—role in drug metabolism and potential drug target?Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.