. . . . . . . . . . . . "[Out of 36 achromats, 12 (33%) had mutations in CNGB3 (six different mutations including four novel mutations)/should be considered as a candidate gene to be evaluated in patients with forms of cone dysfunction, including macular degeneration.]. 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 . "2016-05-13T12:43:21+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .