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

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書目詳細資料
發表在:Front Endocrinol (Lausanne)
Main Authors: Pignatelli, Duarte, Carvalho, Berta L., Palmeiro, Aida, Barros, Alberto, Guerreiro, Susana G., Macut, Djuro
格式: Artigo
語言:Inglês
出版: Frontiers Media S.A. 2020
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7065038/
https://ncbi.nlm.nih.gov/pubmed/32194508
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2020.00113
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