Please use this identifier to cite or link to this item:
Type: Resumo
Title: A Novel Cyp21a2 Mutation Identified A Patient With Classical 21-hydroxylase Deficiency
Author: Michelato
Dd P.; Petroli
R. J.; Santos
L. Gd; Monlleo
I. L.; Mello
M. Pd
Editor: Karger
Citation: Hormone Research In Paediatrics. Karger, v. 86, p. 75 - 75, 2016.
Rights: fechado
Identifier DOI: 10.1159/000451040
Date Issue: 2016
Appears in Collections:Unicamp - Artigos e Outros Documentos

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