Dual Heterozygous Mutations in CYP21A2 and CYP11B1 in a Case of Nonclassic Congenital Adrenal Hyperplasia
Author:
Publisher
Elsevier BV
Subject
Endocrinology, Diabetes and Metabolism
Reference20 articles.
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2. Extensive clinical experience: nonclassical 21-hydroxylase deficiency;New;J Clin Endocrinol Metab,2006
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5. Serum 21-Deoxycortisol, 17-Hydroxyprogesterone, and 11-Deoxycortisol in Classic Congenital Adrenal Hyperplasia: Clinical and Hormonal Correlations and Identification of Patients with 11β-Hydroxylase Deficiency among a Large Group with Alleged 21-Hydroxylase Deficiency
Cited by 3 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 with Combined 21-hydroxylase deficiency and 17α-hydroxylase/17,20-lyase deficiency: An undervirilized male;European Journal of Medical Genetics;2024-06
2. Non-Classic Congenital Adrenal Hyperplasia in Childhood: A Review;Sexes;2023-09-25
3. Editorial for November/December Issue of AACE Clinical Case Reports;AACE Clinical Case Reports;2022-11
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