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Article

Molecular background and clinical characteristics of HNF1A MODY in a Polish population.

Diabetes & metabolism - 1 Nov 2008

Skupien J, Gorczynska-Kosiorz S, Klupa T, Cyganek K, Wanic K, Borowiec M, Sieradzki J, Malecki M-T

Abstract excerpt

PURPOSE: Knowing the molecular background of monogenic diabetes in affected individuals influences the clinical practice. Mutations in the HNF1A gene are the most frequent cause of MODY. The aim of the present study was to identify the genetic and clinical characteristics of HNF1A MODY in a Polish population, and the prevalence of diabetic complications and renal malformations. METHODS: We identified 47 families...

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PMID: 18838325
DOI: 10.1016/j.diabet.2008.05.004

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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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