Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels. [PDF]
Doleschall M +13 more
europepmc +1 more source
Mutations of P450c21 (steroid 21-hydroxylase) at Cys428, Val281, and Ser268 result in complete, partial, or no loss of enzymatic activity, respectively. [PDF]
Da Wu, Bon‐chu Chung
openalex +1 more source
Nonisotopic detection of point mutations in CYP21B gene in steroid 21-hydroxylase deficiency [PDF]
Begoña Ezquieta +4 more
openalex +1 more source
Congenital adrenal hyperplasia due to steroid 21‐hydroxylase deficiency [PDF]
Phyllis Speiser, Perrin C. White
openalex +1 more source
CH-8 Phenotype in Steroid 21-Hydroxylase Deficiency: Fact or Fancy? [PDF]
Hsien-Hsiung Lee
openalex +1 more source
Regulation of Extraadrenal Steroid 21-Hydroxylase Activity [PDF]
Paul C. MacDonald +4 more
openaire +1 more source
Determination of 14 steroid hormones in amniotic fluid (AF): its usefulness in the antenatal diagnosis of 21-hydroxylase deficiency [PDF]
Maguelone G. Forest +4 more
openalex +1 more source
Human Cytochrome P450 21A2, the Major Steroid 21-Hydroxylase: STRUCTURE OF THE ENZYME·PROGESTERONE SUBSTRATE COMPLEX AND RATE-LIMITING C-H BOND CLEAVAGE. [PDF]
Pallan PS +7 more
europepmc +1 more source

