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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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dc.contributor.authorPignatelli, Duarte (7004650708)
dc.contributor.authorCarvalho, Berta L. (36187936200)
dc.contributor.authorPalmeiro, Aida (57225289514)
dc.contributor.authorBarros, Alberto (15847579700)
dc.contributor.authorGuerreiro, Susana G. (15725203500)
dc.contributor.authorMacut, Djuro (35557111400)
dc.date.accessioned2025-06-12T14:27:42Z
dc.date.available2025-06-12T14:27:42Z
dc.date.issued2020
dc.description.abstractIn 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.
dc.identifier.urihttps://doi.org/10.3389/fendo.2020.00113
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85083264097&doi=10.3389%2ffendo.2020.00113&partnerID=40&md5=58c02cba51e83f245496e20c13d2f337
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/4958
dc.subject21OH deficiency
dc.subjectadrenal cortex
dc.subjectandrogen excess syndromes
dc.subjectCAH—congenital adrenal hyperplasia
dc.subjectdisorders of sex development
dc.subjectendocrine genetics
dc.subjectgenotyping
dc.subjectrare diseases
dc.titleCorrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency (Front. Endocrinol., (2019), 10, (432), 10.3389/fendo.2019.00432)
dspace.entity.typePublication

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