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Authors: V. Sulmont
Journal Article
Phenotype-Genotype Correlations of 13 Rare CYP21A2 Mutations Detected in 46 Patients Affected with 21-Hydroxylase Deficiency and in One Carrier Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 95, Issue 3, 1 March 2010, Pages 1288–1300, https://doi.org/10.1210/jc.2009-1202
Published: 01 March 2010
