Please use this identifier to cite or link to this item:
https://hdl.handle.net/10216/145290
Author(s): | Pignatelli, D Carvalho, B Palmeiro, A Barros, A Guerreiro, SG Macut, D |
Title: | Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency |
Publisher: | Frontiers Media |
Issue Date: | 2020 |
Subject: | 21OH deficiency adrenal cortex androgen excess syndromes CAH—congenital adrenal hyperplasia disorders of sex development endocrine genetics genotyping rare diseases |
URI: | https://hdl.handle.net/10216/145290 |
Source: | Frontiers in Endocrinology, vol.11:113 |
Document Type: | Outra Publicação em Revista Científica Internacional |
Rights: | openAccess |
Appears in Collections: | I3S - Outra Publicação em Revista Científica Internacional |
Files in This Item:
File | Description | Size | Format | |
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10.3389-fendo.2020.00113.pdf | 79.79 kB | Adobe PDF | ![]() View/Open |
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