Structure of human steroid 21-hydroxylase genes.

Lignende værker

• Frequent deletion and duplication of the steroid 21-hydroxylase genes.
  af: Werkmeister, J W, et al.
  Udgivet: (1986)
• Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.
  af: White, P C, et al.
  Udgivet: (1988)
• Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.
  af: White, P C, et al.
  Udgivet: (1985)
• High frequency of nonclassical steroid 21-hydroxylase deficiency.
  af: Speiser, P W, et al.
  Udgivet: (1985)
• Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.
  af: Amor, M, et al.
  Udgivet: (1988)