Structure of human steroid 21-hydroxylase genes.

Eitemau Tebyg

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