17 alpha-hydroxylase/17,20-lyase deficiency: from clinical investigation to molecular definition

Endocr Rev. 1991 Feb;12(1):91-108. doi: 10.1210/edrv-12-1-91.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Adrenal Hyperplasia, Congenital* / enzymology
  • Adrenal Hyperplasia, Congenital* / genetics
  • Adrenal Hyperplasia, Congenital* / pathology*
  • Aldehyde-Lyases / deficiency*
  • Aldehyde-Lyases / genetics
  • Amino Acid Sequence
  • Base Sequence
  • Cytochrome P-450 Enzyme System / deficiency*
  • Cytochrome P-450 Enzyme System / genetics
  • Humans
  • Molecular Sequence Data
  • Steroid 17-alpha-Hydroxylase / genetics

Substances

  • Cytochrome P-450 Enzyme System
  • Steroid 17-alpha-Hydroxylase
  • Aldehyde-Lyases