Amino Acid Residue 147 of Human Aldosterone Synthase and 11 -Hydroxylase Plays a Key Role in 11 -Hydroxylation
Author:
Publisher
The Endocrine Society
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The molecular basis and genotype–phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population;Molecular Biology Reports;2019-04-20
2. Effects of genetic variation in the aldosterone synthase (CYP11B2) gene on enzyme function;Clinical Endocrinology;2009-03
3. Polymorphic Variation in the 11β-Hydroxylase Gene Associates With Reduced 11-Hydroxylase Efficiency;Hypertension;2007-01
4. Functional effects of genetic variants in the 11?-hydroxylase (CYP11B1) gene;Clinical Endocrinology;2006-12
5. Neonatal salt-wasting and 11 β-hydroxylase deficiency in a child carrying a homozygous deletion hybrid CYP11B2 (aldosterone synthase)-CYP11B1 (11 β-hydroxylase);Clinical Genetics;2004-06-25
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