@inproceedings{inproceedingsa0127f9b,
title   = {Whole exome sequencing identifies a homozygous mutation in nicotinamide nucleotide transidrogenase as the cause of familial glucocorticoid deficiency},
author = {Bodoni, Aline Faccioli and Coeli-Lacchini, Fernanda Borchers and Souza, Jorge Estefano de and Moreira, Ayrton Custódio and Elias, Lucila Leico Kagohara and Silva Júnior, Wilson Araújo da and Castro, Margaret de and Antonini, Sonir Roberto Rauber},
year = {2015},
publisher = {SBEM},
booktitle   = {Congresso Paulista de Endocrinologia e Metabologia - COPEM}
}