. . . . . . . "[GLDC or AMT mutations were identified in 75% of neonatal and 83% of infantile families, but not in late-onset type NKH.]. 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 . "2017-10-17T13:10:27+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .