. . . . . . . "[We performed molecular genetic analysis of the CYP11B1 gene in six patients with preliminary clinical diagnosis of 11?-OHD and four patients identified as potential 11?-OHD from a CAH cohort in which CYP21A2 gene mutations consecutively screened.]. 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 . "2017-10-17T13:11:55+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .