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

Detalles Bibliográficos
Autores principales: Pignatelli, Duarte, Carvalho, Berta L., Palmeiro, Aida, Barros, Alberto, Guerreiro, Susana G., Macut, Djuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065038/
https://www.ncbi.nlm.nih.gov/pubmed/32194508
http://dx.doi.org/10.3389/fendo.2020.00113
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author Pignatelli, Duarte
Carvalho, Berta L.
Palmeiro, Aida
Barros, Alberto
Guerreiro, Susana G.
Macut, Djuro
author_facet Pignatelli, Duarte
Carvalho, Berta L.
Palmeiro, Aida
Barros, Alberto
Guerreiro, Susana G.
Macut, Djuro
author_sort Pignatelli, Duarte
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spelling pubmed-70650382020-03-19 Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency Pignatelli, Duarte Carvalho, Berta L. Palmeiro, Aida Barros, Alberto Guerreiro, Susana G. Macut, Djuro Front Endocrinol (Lausanne) Endocrinology Frontiers Media S.A. 2020-03-04 /pmc/articles/PMC7065038/ /pubmed/32194508 http://dx.doi.org/10.3389/fendo.2020.00113 Text en Copyright © 2020 Pignatelli, Carvalho, Palmeiro, Barros, Guerreiro and Macut. http://creativecommons.org/licenses/by/4.0/ 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.
spellingShingle Endocrinology
Pignatelli, Duarte
Carvalho, Berta L.
Palmeiro, Aida
Barros, Alberto
Guerreiro, Susana G.
Macut, Djuro
Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
title Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
title_full Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
title_fullStr Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
title_full_unstemmed Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
title_short Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
title_sort corrigendum: the complexities in genotyping of congenital adrenal hyperplasia: 21-hydroxylase deficiency
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065038/
https://www.ncbi.nlm.nih.gov/pubmed/32194508
http://dx.doi.org/10.3389/fendo.2020.00113
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