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Article

Analysis of TPO gene in Turkish children with iodide organification defect: identification of a novel mutation.

Endocrine - 1 Feb 2010

Turkkahraman Doga, Alper Ozgul M, Pehlivanoglu Suray, Aydin Funda, Yildiz Akin, Luleci Guven, Akcurin Sema, Bircan Iffet

Abstract excerpt

The objective was to determine molecular genetic analysis of the TPO gene in Turkish children with iodide organification defect (IOD). Patients with a diagnosis of primary hypothyroidism were evaluated. Subjects having a definite diagnosis of autoimmune thyroiditis, thyroid gland dysplasia and, or iodine deficiency were excluded. A total of 10 patients from nine unrelated Turkish families, with an unknown...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20963560
DOI: 10.1007/s12020-009-9280-1

Genes

TPO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Analysis of TPO gene in Turkish children with iodide organification defect: identification of a novel mutation.PMID 20963560Read ↗

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