. . . . . . . "[Except for the neonatal CH due to biallelic TSH? mutations, the thyroid hormone defect is rarely as profound as can be observed in some primary forms.]. 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 . "2017-10-17T13:17:04+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .