. . . . . . . . . . . . "[The c.61C>T (p.R21W) mutation in CRYAA has been previously reported in a family with congenital cataract and microcornea.]. 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 . "2016-05-13T12:49:45+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .