. . . . . . . "[The function of DUOX2 in thyroid hormonogenesis has been firmly established by linking the congenital hypothyroid phenotype 'total iodide organification defect' to biallelic inactivating DUOX2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:18:27+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .