. . . . . . . "[Mutation screening of the candidate genes detected a heterozygous c.465G ? C change in the exon6 of the ?B2-crystallin gene (CRYBB2) in all family members affected with cataracts, resulting in the substitution of a highly conserved Tryptophan to Cystine (p.W151C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:11:45+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .