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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
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 diseasesMore Related Videos
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