. . . . . . . "[The effects of three mutations in SCN1A have been characterized in cultured mammalian cells as a gain-of-function abnormality causing prolonged membrane depolarization, a plausible underlying biophysical mechanism responsible for inherited epilepsy.]. 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 . "2017-10-17T13:16:04+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .