. . . . . . . "[In this longitudinal study, 58 subjects were identified who had at least two MRI and MAPT mutations (n�=�21), GRN mutations (n�=�11), C9ORF72 repeat expansions (n�=�11) or sporadic FTD (n�=�15).]. 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 . "2017-10-17T13:14:25+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .