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Article

Permanent neonatal diabetes: different aetiology in Arabs compared to Europeans.

Archives of disease in childhood - 1 Aug 2012

Habeb Abdelhadi M, Flanagan Sarah E, Deeb Asma, Al-Alwan Ibrahim, Alawneh Hussain, Balafrej Angham A L, Mutair Angam, Hattersley Andrew T, Hussain Khalid, Ellard Sian

Abstract excerpt

OBJECTIVE: Mutations in the KCNJ11 and ABCC8 genes that encode the pancreatic K(ATP) channel are the commonest cause of permanent neonatal diabetes mellitus (PNDM). The authors aimed to define the genetic causes of PNDM in a large cohort of Arab patients and compare them with a British cohort tested in the same laboratory. DESIGN: Retrospective observational study. SETTING: International genetics centre....

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Potassium Channels, Inwardly Rectifying

Source

Identifiers

PMID: 22859427
DOI: 10.1136/archdischild-2012-301744

Genes

KCNJ11
ABCC8
GCK
INS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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