Partial Defect in the Cholesterol Side-Chain Cleavage Enzyme P450scc (CYP11A1) Resembling Nonclassic Congenital Lipoid Adrenal Hyperplasia
Author:
Affiliation:
1. Department of Pediatrics (T.S., M.K.T., W.L.M.), University of California, San Francisco, San Francisco, California 94143;
2. Department of Pediatrics (P.R.B.), University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Link
http://academic.oup.com/jcem/article-pdf/96/3/792/9068450/jcem0792.pdf
Reference42 articles.
1. Human cholesterol side-chain cleavage enzyme, P450scc: cDNA cloning, assignment of the gene to chromosome 15, and expression in the placenta.;Chung;Proc Natl Acad Sci USA,1986
2. Gene structure of human cytochrome P-450(SCC), cholesterol desmolase.;Morohashi;J Biochem,1987
3. Regional mapping of genes encoding human steroidogenic enzymes: P450scc to 15q23-q24, adrenodoxin to 11q22; adrenodoxin reductase to 17q24-q25; and P450c17 to 10q24-q25.;Sparkes;DNA Cell Biol,1991
4. Minireview: regulation of steroidogenesis by electron transfer.;Miller;Endocrinology,2005
5. Congenital lipoid adrenal hyperplasia: the human gene knockout for the steroidogenic acute regulatory protein.;Miller;J Mol Endocrinol,1997
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