. . . . . . . . . . . . "[In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis of an inherited speech and language disorder suffered by members of the family known as KE. This mini-symposium review focuses on recent findings and research-in-progress, primarily from five laboratories.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:46:05+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .