Screening of Novel Candidate Compounds for the Treatment of Primary Aldosteronism
Author:
Publisher
Elsevier BV
Reference35 articles.
1. Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review;H Miao;Steroids,2019
2. Characterization of human adrenal cytochrome P450 11B2 products of progesterone and androstenedione oxidation;S M Glass;J Steroid Biochem Mol Biol,2021
3. Immunohistochemistry of the Human Adrenal CYP11B2 in Normal Individuals and in Patients with Primary Aldosteronism;C E Gomez-Sanchez;Horm Metab Res,2020
4. Abdulsalam Abu-Libdeh, Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity;E H Yaniv Faingelernt;American journal of medical genetics,2021
5. & Kanaka-Gantenbein, C, Molecular Analysis of the CYP11B2 Gene in 62 Patients with Hypoaldosteronism Due to Aldosterone Synthase Deficiency;C Merakou;The Journal of clinical endocrinology and metabolism,2021
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