Title | Date | PubMed ID |
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The impact of the clinical CYP11B2 mutation V386A strongly depends on the enzyme's genetic background. | 2017 Apr 29 | 28190867 |
Congenital hypoaldosteronism. | 2008 Aug | 18723916 |
CMO I deficiency caused by a point mutation in exon 8 of the human CYP11B2 gene encoding steroid 18-hydroxylase (P450C18). | 1997 May 19 | 9177280 |
Studies on aldosterone biosynthesis in vitro. | 1966 Jun | 4381410 |