. . . . . . . "[Because FHM gene mutations were also found in family members with 'nonhemiplegic' typical migraine with and without aura, our findings reinforce the hypothesis that FHM, SHM, and 'normal' migraine are part of a disease spectrum with shared pathogenetic mechanisms.]. 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 . "2017-10-17T13:11:10+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .