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

AuthID
P-00Q-SK3
6
Author(s)
Tipo de Documento
Review
Year published
2019
Publicado
in FRONTIERS IN ENDOCRINOLOGY, ISSN: 1664-2392
Volume: 10, Número: JULY
Indexing
Publication Identifiers
SCOPUS: 2-s2.0-85069452448
Wos: WOS:000474257500001
Source Identifiers
ISSN: 1664-2392
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