. . . . . . . "[identified the novel p.L1649Q mutation (c.4946T > A) in SCN1A in a North American kindred with familial hemiplegic migraine without associated ataxia or epilepsy; findings establish role of neuronal Na (v) 1.1 sodium channels in FHM]. 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" .