[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.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE