. . . . . . . "[The major mutation is a 1.02 kb deletion, which removes exons 7 and 8/homozygotic and heterozygotic deletions at the CLN3 gene site have been associated with the clinical syndromes of juvenile neuronal ceroid-lipofuscinosis.]. 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 . "2017-10-17T13:11:36+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .