. . . . . . . . . . . . "[We detected an additional previously uncharacterized mutation: R384G mutation, a single C-->G base substitution in the codon 384 of the exon 7 changing an arginine (CGA) to a glycine (GGA) by sequencing the CYP11B1 gene of Japanese siblings with 11 beta-OHD.]. 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 . "2014-10-02T12:34:25+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .