P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia.

Congenital adrenal hyperplasia (CAH) is a common genetic disorder due to defective 21-hydroxylation of steroid hormones. The human P450XXIA2 gene encodes cytochrome P450c21 [steroid 21-monooxygenase (steroid 21-hydroxylase), EC 1.14.99.10], which mediates 21-hydroxylation. The P450XXIA2 gene may be...

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Pubblicato in:	Proc Natl Acad Sci U S A
Autori principali:	Matteson, K J, Phillips, J A, Miller, W L, Chung, B C, Orlando, P J, Frisch, H, Ferrandez, A, Burr, I M
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	National Academy of Sciences 1987
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC298962/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3497399/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.84.16.5858
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