Steroid 11β-Hydroxylase Deficiency and Related Disorders
Author:
Funder
National Institutes of Health
Publisher
Elsevier
Reference121 articles.
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4. The synthesis of aldosterone by the adrenal cortex. Two zones (fasciculata and glomerulosa) possess one enzyme for 11 beta-, 18- hydroxylation, and aldehyde synthesis;Yanagibashi;J Biol Chem,1986
5. Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta);Mornet;J Biol Chem,1989
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1. Disorders of the Adrenal Cortex in the Fetus and Neonate;Maternal-Fetal and Neonatal Endocrinology;2020
2. Monogenic Hypertension;Secondary Hypertension;2019-12-12
3. 11β-Hydroxylase deficiency detected by urine steroid metabolome profiling using gas chromatography-mass spectrometry;Clinical Mass Spectrometry;2018-01
4. Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency;Proceedings of the National Academy of Sciences;2017-02-22
5. Novel and prevalent CYP11B1 gene mutations in Turkish patients with 11-β hydroxylase deficiency;The Journal of Steroid Biochemistry and Molecular Biology;2017-01
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