. . . . . . . "[The mutation IVS2 -2A-- > C of SEDL gene was firstly determined in the world/change of the splice acceptor in SEDL intron 2 may cause skipping of exon 3 which is responsible for the X-linked spondyloepiphyseal dysplasia tarda.]. 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 . "2017-10-17T13:16:09+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .