. . . . . . . "[FOXP2 is disrupted by a translocation in CS, a child with severe speech/language disorder/, a point mutation, altering a critical residue of the forkhead domain, segregates with speech/language deficits in all 15 affected members of family KE.]. 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 . "2017-10-17T13:19:02+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .