X-Linked Adrenal Hypoplasia Congenita Caused by a Novel Intronic Mutation of the DAX-1 Gene
Author:
Publisher
S. Karger AG
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Cited by 8 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. Novel non-stop variant of the NR0B1 gene in two siblings with adrenal hypoplasia congenita;Journal of Pediatric Endocrinology and Metabolism;2022-07-14
2. Adrenal hypoplasia congenita in identical twins;Saudi Medical Journal;2019-01
3. Identification of NR0B1 as a novel androgen receptor co-repressor in mouse Sertoli cells;International Journal of Molecular Medicine;2016-07-11
4. The analysis of clinical manifestations and genetic mutations in Chinese boys with primary adrenal insufficiency;Journal of Pediatric Endocrinology and Metabolism;2012-01-01
5. Genetic Analysis ofNR0B1in Congenital Adrenal Hypoplasia Patients: Identification of a Rare Regulatory Variant Resulting in Congenital Adrenal Hypoplasia and Hypogonadal Hypogonadism without Testicular Carcinoma in situ;Sexual Development;2012
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