. . . . . . . . . . . . "[Patients were classified according to age of onset, clinical pattern, and associated neurological signs into 'ULD-like' and 'not ULD-like.' After exclusion of mutations in cystatin B (CSTB), DNA was examined for sequence variation in SCARB2 and PRICKLE1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-27"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:40:52+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .