We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleCongenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene.AuthorsPfarr, Nicole; Korsch, Eckhard; Kaspers, Stefan; Herbst, Antje; Stach, Armin; Zimmer, Claudia; Pohlenz, JoachimAbstractCongenital primary hypothyroidism (CH) occurs in one of 4000 births and in 20% of the cases CH is due to a defect in thyroid hormonogenesis. Candidate genes were examined to determine the precise aetiology of suspected dyshormonogenesis in CH.PublicationClinical endocrinology, 2006, Vol 65, Issue 6, p810ISSN0300-0664Publication typeJournal ArticleDOI10.1111/j.1365-2265.2006.02672.x