Variable clinical phenotypes in a family with homozygous c.1159G>A mutation in the thyroid peroxidase gene

Lee CC 1 , Harun F , Jalaludin MY , Heh CH , Othman R , Kang IN Show all authors , Mat Junit S

Affiliations 

  • 1 Department of Molecular Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
Horm Res Paediatr, 2014;81(5):356-60.
PMID: 24717978 DOI: 10.1159/000359922

Abstract

Defects in the thyroid peroxidase (TPO) gene have been associated with goitrous congenital hypothyroidism (CH).

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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