Molecular basis of congenital adrenal hyperplasia due to 3 beta- hydroxysteroid dehydrogenase deficiency
Author:
Publisher
The Endocrine Society
Subject
Endocrinology,Molecular Biology,General Medicine
Cited by 108 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. 3β-Hydroxysteroid Dehydrogenase Type 2 (3βHSD2) Deficiency due to a Novel Compound Heterozygosity of a Missense Mutation (p.Thr259Met) and Frameshift Deletion (p.Lys273ArgFs*7) in an Undervirilized Infant Male with Salt Wasting;Sexual Development;2021-10-08
2. Three cases of 3β-hydroxysteroid dehydrogenase deficiency: Clinical analysis;Advances in Clinical and Experimental Medicine;2021-03-23
3. Disorders of the Adrenal Cortex in the Fetus and Neonate;Maternal-Fetal and Neonatal Endocrinology;2020
4. The molecular basis and genotype–phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population;Molecular Biology Reports;2019-04-20
5. Clinical perspectives in congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase type 2 deficiency;Endocrine;2019-02-04
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