Publication: Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency (Front. Endocrinol., (2019), 10, (432), 10.3389/fendo.2019.00432)
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Date
2020
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Abstract
In the article, an author’s name was incorrectly spelled as Djuro Maçut. The correct spelling is Djuro Macut. In addition there was an error in affiliation 7. Instead of “Department of Endocrinology, Diabetes and Metabolic Diseases, Faculty of Medicine, University of Belgrade, Belgrade, Serbia,” it should be “Clinic of Endocrinology, Diabetes and Metabolic Diseases, Faculty ofMedicine, University of Belgrade, Belgrade, Serbia.” The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated. © Copyright © 2020, Pignatelli, Carvalho, Palmeiro, Barros, Guerreiro and Macut.
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Keywords
21OH deficiency, adrenal cortex, androgen excess syndromes, CAH—congenital adrenal hyperplasia, disorders of sex development, endocrine genetics, genotyping, rare diseases
