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.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.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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