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Article

[Three-year observation of permanent neonatal diabetes].

Pediatric endocrinology, diabetes, and metabolism - 1 Jan 2010

Noczyńska Anna, Zubkiewicz-Kucharska Agnieszka, Salmonowicz Barbara, Małecki Maciej, Młynarski Wojciech

Abstract excerpt

The aim of this paper is to present a three-year observation of four children with permanent neonatal diabetes caused by heterozygous activating mutations in both KCNJ11 gene for Kir6.2 and ABCC8 gene for SUR1 subunits (three patients after three years of clinical observation and one patient afte...

Read the complete abstract on PubMed

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Share to ATP-Binding Cassette Transporters
Share to Diabetes Mellitus, Type 1
Share to Hypoglycemic Agents

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

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Share to Potassium Channels, Inwardly Rectifying

Share to Receptors, Drug

Share to Sulfonylurea Receptors

Source

Identifiers

PMID: 20529607

Genes

ABCC8
KCNJ11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20529607-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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