Frontiers in Endocrinology (Mar 2020)
Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
- Duarte Pignatelli,
- Duarte Pignatelli,
- Duarte Pignatelli,
- Berta L. Carvalho,
- Berta L. Carvalho,
- Aida Palmeiro,
- Alberto Barros,
- Alberto Barros,
- Susana G. Guerreiro,
- Susana G. Guerreiro,
- Djuro Macut
Affiliations
- Duarte Pignatelli
- Hospital S. João, Porto, Portugal
- Duarte Pignatelli
- Department of Biomedicine, Faculty of Medicine of Porto, Porto, Portugal
- Duarte Pignatelli
- IPATIMUP/I3S Research Institute, University of Porto, Porto, Portugal
- Berta L. Carvalho
- Genetics, Department of Pathology, Faculty of Medicine, University of Porto, Porto, Portugal
- Berta L. Carvalho
- I3S Research Institute, University of Porto, Porto, Portugal
- Aida Palmeiro
- Clinical Genetics Center, Porto, Portugal
- Alberto Barros
- Genetics, Department of Pathology, Faculty of Medicine, University of Porto, Porto, Portugal
- Alberto Barros
- I3S Research Institute, University of Porto, Porto, Portugal
- Susana G. Guerreiro
- Department of Biomedicine, Faculty of Medicine of Porto, Porto, Portugal
- Susana G. Guerreiro
- IPATIMUP/I3S Research Institute, University of Porto, Porto, Portugal
- Djuro Macut
- Clinic of Endocrinology, Diabetes and Metabolic Diseases, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
- DOI
- https://doi.org/10.3389/fendo.2020.00113
- Journal volume & issue
-
Vol. 11
Abstract
No abstracts available.Keywords
- 21OH deficiency
- CAH—congenital adrenal hyperplasia
- adrenal cortex
- androgen excess syndromes
- genotyping
- endocrine genetics
