Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene
Coeli, Fernanda Borchers, Ferraz, Lúcio Fábio Caldas, Lemos-Marini, Sofia H. V. de, Rigatto, Sumara Zuanazi Pinto, Belangero, Vera Maria Santoro, de-Mello, Maricilda PalandiVolume:
52
Journal:
Arquivos Brasileiros de Endocrinologia & Metabologia
DOI:
10.1590/s0004-27302008000800012
Date:
November, 2008
File:
PDF, 175 KB
2008