. . . . . . . "[A high frequency of MD from mutations in GCK/HNF1? may be identified among pediatric diabetic patients originally considered to have T1D by performing genetic testing on those patients with multiple clinical risk factors for MD.]. 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 . "2017-10-17T13:16:34+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .