. . . . . . . . . . . . "[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 . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:47:34+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .