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Late diagnosis of partial 3β-hydroxysteroid dehydrogenase type 2 deficiency - characterization of a new genetic variant.
Øzdemir CM, Nielsen MM, Liimatta J, Voegel CD, Elzenaty RN, Wasehuus VS, Lind-Holst M, Ornstrup MJ, Gram SB, Ousager LB, Flück CE, Gravholt CH. Øzdemir CM, et al. Among authors: wasehuus vs. Endocrinol Diabetes Metab Case Rep. 2024 Aug 1;2024(3):23-0090. doi: 10.1530/EDM-23-0090. Print 2024 Jul 1. Endocrinol Diabetes Metab Case Rep. 2024. PMID: 39089319 Free PMC article.