1. Repositório Aberto da Universidade do Porto
  2. I3S - Instituto de Investigação e Inovação em Saúde
  3. I3S - Outra Publicação em Revista Científica Internacional
Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/145290
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DC FieldValueLanguage
dc.creatorPignatelli, D-
dc.creatorCarvalho, B-
dc.creatorPalmeiro, A-
dc.creatorBarros, A-
dc.creatorGuerreiro, SG-
dc.creatorMacut, D-
dc.date.accessioned2022-11-17T11:40:27Z-
dc.date.available2022-11-17T11:40:27Z-
dc.date.issued2020-
dc.identifier.issn1664-2392-
dc.identifier.urihttps://hdl.handle.net/10216/145290-
dc.language.isoeng-
dc.publisherFrontiers Media-
dc.relation.ispartofFrontiers in Endocrinology, vol.11:113-
dc.rightsopenAccess-
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-
dc.typeOutra Publicação em Revista Científica Internacional-
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde-
dc.identifier.doi10.3389/fendo.2020.00113-
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fendo.2020.00113/full-
Appears in Collections:I3S - Outra Publicação em Revista Científica Internacional

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