Synergistic Effect of Partially Inactivating Mutations in Steroid 21-Hydroxylase Deficiency
Author:
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 58 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. Genetic profiling of CAH Egyptian children: rapid guide to clinical interpretation of common mutations;Journal of Endocrinological Investigation;2020-05-01
2. Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia;Clinical Biochemistry;2019-11
3. The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency;Frontiers in Endocrinology;2019-07-04
4. CYP21A2mutation update: Comprehensive analysis of databases and published genetic variants;Human Mutation;2017-11-06
5. Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women;Human Reproduction Update;2017-06-05
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