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

Duarte Pignatelli; Berta L Carvalho; Aida Palmeiro; Alberto Barros; Susana G Guerreiro; Djuro Macut

doi:10.3389/fendo.2020.00113

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

Front Endocrinol (Lausanne). 2020 Mar 4:11:113. doi: 10.3389/fendo.2020.00113. eCollection 2020.

Authors

Duarte Pignatelli^{1

2

3}, Berta L Carvalho^{4

5}, Aida Palmeiro⁶, Alberto Barros^{4

5}, Susana G Guerreiro^{2

3}, Djuro Macut⁷

Affiliations

¹ Hospital S. João, Porto, Portugal.
² Department of Biomedicine, Faculty of Medicine of Porto, Porto, Portugal.
³ IPATIMUP/I3S Research Institute, University of Porto, Porto, Portugal.
⁴ Genetics, Department of Pathology, Faculty of Medicine, University of Porto, Porto, Portugal.
⁵ I3S Research Institute, University of Porto, Porto, Portugal.
⁶ Clinical Genetics Center, Porto, Portugal.
⁷ Clinic of Endocrinology, Diabetes and Metabolic Diseases, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Abstract

[This corrects the article on p. 432 in vol. 10, PMID: 31333583.].

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

Publication types

Published Erratum