[This study was designed to define the prevalence of CH due to mutations of PAX8, NKX2-1 encoding thyroid transcription factor (TTF)-1, FOXE1 (encoding TTF-2), and NKX2-5 among patients with permanent primary CH and in the general population in Japan.]. 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