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Authors: Jens Commentz
Journal Article
Congenital Adrenal Hyperplasia Due to 11-Hydroxylase Deficiency: Functional Characterization of Two Novel Point Mutations and a Three-Base Pair Deletion in the CYP11B1 Gene Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 90, Issue 6, 1 June 2005, Pages 3724–3730, https://doi.org/10.1210/jc.2005-0089
Published: 01 June 2005
