Characterization of the consequence of a novel Glu-380 to Asp mutation by expression of functional P450c21 in Escherichia coli
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics,Structural Biology
Reference32 articles.
1. Physiology and Molecular Biology of P450c21 and P450c17
2. THE MOLECULAR GENETICS OF 21-HYDROXYLASE DEFICIENCY
3. Structure of human steroid 21-hydroxylase genes
4. Clinical and Molecular Genetics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
5. Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Cited by 6 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. Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase Deficiency: A Comprehensive Focus on 233 Pathogenic Variants of CYP21A2 Gene;Molecular Diagnosis & Therapy;2018-02-15
2. CYP21A2mutation update: Comprehensive analysis of databases and published genetic variants;Human Mutation;2017-11-06
3. Molecular Model of Human CYP21 Based on Mammalian CYP2C5: Structural Features Correlate with Clinical Severity of Mutations Causing Congenital Adrenal Hyperplasia;Molecular Endocrinology;2006-11-01
4. CYP21mutations and congenital adrenal hyperplasia;Clinical Genetics;2001-05
5. Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency;Endocrine Reviews;2000-06-01
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