TitleDatePubMed ID
The impact of the clinical CYP11B2 mutation V386A strongly depends on the enzyme's genetic background.2017 Apr 2928190867
Congenital hypoaldosteronism.2008 Aug18723916
CMO I deficiency caused by a point mutation in exon 8 of the human CYP11B2 gene encoding steroid 18-hydroxylase (P450C18).1997 May 199177280
Studies on aldosterone biosynthesis in vitro.1966 Jun4381410