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CORRECTION article

Front. Endocrinol., 04 March 2020
Sec. Systems Endocrinology
Volume 11 - 2020 | https://doi.org/10.3389/fendo.2020.00113
This article is part of the Research Topic Congenital Adrenal Hyperplasia, Unresolved Issues and Implications on Clinical Management View all 11 articles

Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency

This article is a correction to:

  1. The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency

    1. Read original article
\nDuarte Pignatelli,, Duarte Pignatelli1,2,3*Berta L. Carvalho,Berta L. Carvalho4,5Aida PalmeiroAida Palmeiro6Alberto Barros,Alberto Barros4,5Susana G. Guerreiro,Susana G. Guerreiro2,3Djuro MacutDjuro Macut7
  • 1Hospital S. João, Porto, Portugal
  • 2Department of Biomedicine, Faculty of Medicine of Porto, Porto, Portugal
  • 3IPATIMUP/I3S Research Institute, University of Porto, Porto, Portugal
  • 4Genetics, Department of Pathology, Faculty of Medicine, University of Porto, Porto, Portugal
  • 5I3S Research Institute, University of Porto, Porto, Portugal
  • 6Clinical Genetics Center, Porto, Portugal
  • 7Clinic of Endocrinology, Diabetes and Metabolic Diseases, Faculty of Medicine, University of Belgrade, Belgrade, Serbia

A Corrigendum on
The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency

by Pignatelli, D., Carvalho, B. L., Palmeiro, A., Barros, A., Guerreiro, S. G., and Macut, D. (2019). Front. Endocrinol. 10:432. doi: 10.3389/fendo.2019.00432

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 of Medicine, 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.

Keywords: 21OH deficiency, CAH—congenital adrenal hyperplasia, adrenal cortex, androgen excess syndromes, genotyping, endocrine genetics, rare diseases, disorders of sex development

Citation: Pignatelli D, Carvalho BL, Palmeiro A, Barros A, Guerreiro SG and Macut D (2020) Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency. Front. Endocrinol. 11:113. doi: 10.3389/fendo.2020.00113

Received: 18 February 2020; Accepted: 20 February 2020;
Published: 04 March 2020.

Approved by: Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2020 Pignatelli, Carvalho, Palmeiro, Barros, Guerreiro and Macut. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Duarte Pignatelli, dpignatelli@yahoo.com

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