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

Duarte Pignatelli1,2,3, Berta L Carvalho4,5, Aida Palmeiro6

  • 1Hospital S. João, Porto, Portugal.

Frontiers in Endocrinology
|March 21, 2020
PubMed

Abstract:

[This corrects the article on p. 432 in vol. 10, PMID: 31333583.].

Keywords:
21OH deficiencyCAH—congenital adrenal hyperplasiaadrenal cortexandrogen excess syndromesdisorders of sex developmentendocrine geneticsgenotypingrare diseases

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