Steroid 21-Hydroxylase
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-77763-9_45.pdf
Reference34 articles.
1. Amor M, Parker KL, Globerman H, New MI, White PC (1988) A mutation in the CYP21B gene (Ile-172 to Asn) causes steroid 21-hydroxylase deficiency. Proc Natl Acad Sci USA 85: 1600–1604
2. Carroll MC, Campbell RD, Porter RR (1985) The mapping of 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man. Proc Natl Acad Sci USA 82: 521–525
3. Chaplin DD, Galbraith LJ, Scidman JG, White PC, Parker KL (1986) Nucleotide sequence analysis of murine 21-hydroxylase genes: mutations affecting gene expression. Proc Natl Acad Sci USA 83: 9601–9605
4. Chiou SH, Hu MC, Chung BC (1990) A missense mutation at Ile172→Asn or Arg356→Trp causes steroid 21-hydroxylase deficiency. J Biol Chem 265: 3549–3552
5. Chung BC, Matteson KJ, Miller WL (1986) Structure of a bovine gene for P-450c21 (steroid 21-hydroxylase) defines a novel cytochrome P-450 gene family. Proc Natl Acad Sci USA 83: 4243–4247
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