. . . . . . . . . . . . "[Defects have been associated with chorea, hypothyroidism, and lung disease, comprising the 'brain-thyroid-lung syndrome.' We describe here 3 cases of novel missense mutation (c.626G>C; p.Arg209Pro) in NKX2-1 in 2 generations of a nonconsanguinous family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-27"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:45:06+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .