. . . . . . . "[A number of rare sequence variants in the coding region of the alpha-neurexin 1 leader sequence and of an epidermal growth factor like domain, respectively, suggest that even subtle changes in NRXN1 might contribute to susceptibility to autism.]. 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 . "2017-10-17T13:17:44+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .