A case of primary selective hypoaldosteronism carrying three mutations in the aldosterone synthase (Cyp11b2) gene
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
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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. Neonatal salt wasting syndrome: Aldosterone synthase deficiency caused by a new splicing variant in CYP11B2;Archives de Pédiatrie;2024-02
2. Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review;Steroids;2019-10
3. Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experience;Italian Journal of Pediatrics;2016-08-02
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