. . . . . . . "[We describe a 2-year-old girl affected by SBH with epilepsy and periodic limb movements (PLMs), in whom a novel 'de novo' missense substitution, Met1Val (M1V), was identified in the DCX gene.]. 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 . "2017-10-17T13:11:59+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .