Associated Papers
A Novel NR0B1 Gene Mutation Causes Different Phenotypes in Two Male Patients with Congenital Adrenal Hypoplasia.
Wu SM et al.
Current Medical Science, 2020
The analysis of clinical manifestations and genetic mutations in Chinese boys with primary adrenal insufficiency.
Guoying C et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2012
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