. . . . . . . . . . . . "[(2014) De Novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.Am.J. Hum.Genet., 94, 784-789].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:51:14+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .