Gene symbol: CYP17A1. Disease: Steroid 17-alpha-hydrolylase deficiency

Hum Genet. 2005 May;116(6):539.
No abstract available

MeSH terms

  • Adrenal Hyperplasia, Congenital / genetics*
  • Amino Acid Substitution
  • Humans
  • Mutation, Missense*
  • Steroid 17-alpha-Hydroxylase / genetics
  • Steroid 17-alpha-Hydroxylase / metabolism*

Substances

  • CYP17A1 protein, human
  • Steroid 17-alpha-Hydroxylase