. . . . . . . . . . . . "[To report, for the first time, that X-linked incomplete congenital stationary night blindness (CSNB2A) and Ă…land island eye disease (AIED) phenotypes coexist in a molecularly confirmed pedigree and to present novel phenotypic characteristics of calcium channel alpha-1F subunit gene (CACNA1F)-related disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2014-02-25"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:33:25+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .