Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism
Author:
Publisher
The Endocrine Society
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 73 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. Differences in hormonal levels between heterozygous CYP21A2 pathogenic variant carriers, non-carriers, and females with non-classic congenital hyperplasia;Archives of Endocrinology and Metabolism;2022-03-16
2. 17-Hydroxyprogesterone Response to Standard Dose Synacthen Stimulation Test in CYP21A2 Heterozygous Carriers and Non-carriers in Symptomatic and Asymptomatic Groups: Meta-analyses;Journal of Clinical Research in Pediatric Endocrinology;2022-03-03
3. Should Pediatric Endocrinologists Consider More Carefully When to Perform a Stimulation Test?;Frontiers in Endocrinology;2021-03-22
4. Salt-Losing 21-Hydroxylase Deficiency Caused by Double Homozygosity for Two “Mild” Mutations;The Journal of Clinical Endocrinology & Metabolism;2020-11-27
5. Establishment of Clinical and Lab Algorithms for the Identification of Carriers of Mutations in CYP21A2 – A Study of 365 Children and Adolescents;Experimental and Clinical Endocrinology & Diabetes;2020-08-24
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