. . . . . . . "[Analysis of the CYP21A2 gene in the patients with congenital adrenal hyperplasia from the Republic of Bashkortostan revealed seven different mutations, including deletion/conversion of the delA2orLGC gene, R356W, 12splice, I172N, Q318X, V281L, and P30L.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-21"^^ . . "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" .