. . . . . . . . . . . . "[Primary (familial) HLH is known to occur in children with mutations in perforin, Munc13-4, or syntaxin 11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-27"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:45:45+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .