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Article

Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation.

Diabetologia - 1 Nov 2005

Colombo C, Delvecchio M, Zecchino C, Faienza M F, Cavallo L, Barbetti F

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Share to Diabetes Mellitus
Share to KCNJ11 gene
Share to Glyburide
Share to Hypoglycemic Agents

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Potassium Channels, Inwardly Rectifying

Source

Identifiers

PMID: 16205880
DOI: 10.1007/s00125-005-1958-1

Genes

KCNJ11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation.PMID 16205880Read ↗

Relapsing diabetes can result from moderately activating mutations in KCNJ11.Semantic proximity Read ↗

Activating mutations in Kir6.2 and neonatal diabetes: new clinical syndromes, new scientific insights, and new therapy.Semantic proximity Read ↗

Kir6.2 Mutations Are a Common Cause of Permanent Neonatal Diabetes in a Large Cohort of French PatientsSemantic proximity Read ↗

KCNJ11 activating mutations cause both transient and permanent neonatal diabetes mellitus in Cypriot patients.Semantic proximity Read ↗

[From gene to disease; neonatal diabetes mellitus and the KCNJ11 gene].Semantic proximity Read ↗

[Neonatal diabetes mellitus].Semantic proximity Read ↗

Permanent Neonatal Diabetes due to Mutations in <i>KCNJ11</i> Encoding Kir6.2Semantic proximity Read ↗

Molecular Basis of Neonatal Diabetes Mellitus and Transient Hyperglycemia in the NeonateSemantic proximity Read ↗

Detection of KCNJ11 gene mutations in a family with neonatal diabetes mellitus: implications for therapeutic management of family members with long-standing disease.Semantic proximity Read ↗

Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype.Semantic proximity Read ↗

Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes: new insights and new treatment.Semantic proximity Read ↗

The C42R Mutation in the Kir6.2 (KCNJ11) Gene as a Cause of Transient Neonatal Diabetes, Childhood Diabetes, or Later-Onset, Apparently Type 2 Diabetes MellitusSemantic proximity Read ↗

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