The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency (Vol 10, 432, 2019)

AuthID
 P-00S-02H
6
Author(s)
Palmeiro, A
·
Tipo de Documento
Correction
Year published
2020
Publicado
in FRONTIERS IN ENDOCRINOLOGY, ISSN: 1664-2392
Volume: 11
Indexing
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Scopus®
Crossref®62
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Publication Identifiers
SCOPUS: 2-s2.0-85083264097
Wos: WOS:000525271200001
Source Identifiers
ISSN: 1664-2392
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