CORRIGENDUM: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency (Front. Endocrinol., (2019), 10, (432), 10.3389/Fendo.2019.00432)

AuthID
 P-00S-0CM
6
Author(s)
Pignatelli, D
·
Carvalho, BL
·
Palmeiro, A
·
Guerreiro, SG
·
Macut, D
Document Type
Correction
Year published
2020
Published
in Frontiers in Endocrinology, ISSN: 1664-2392
Volume: 11
Indexing
Scopus®
Google Scholar®
Publication Identifiers
Scopus: 2-s2.0-85083264097
Source Identifiers
ISSN: 1664-2392
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