. . . . . . . . . . . . "[We present a case of permanent neonatal diabetes mellitus due to a C96Y (c.287G > A; p.Cys96Tyr) heterozygous mutation in the insulin (INS) gene/the patient and his father (who had childhood-onset insulin-requiring diabetes) were found to be carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:33:02+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .