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2. Mutation in the CYP21B gene (Ile172 to Asn) causes steroid 21-hydroxylase deficiency;Amor,1988
3. Expression of P1-450 and P3-450 DNA coding sequences as enzymatically active cytochromes P-450 in mammalian cells;Battula,1987
4. 17a-hydroxylation deficiency in man;Biglieri;Journal of Clinical Investigation,1966
5. Late onset adrenocortical hydroxylase deficiencies associated with menstrual dysfunction;Birnbaum;Obstetrics and Gynecology,1984