TY - CPAPER TI - Whole exome sequencing identifies a homozygous mutation in nicotinamide nucleotide transidrogenase as the cause of familial glucocorticoid deficiency PY - 2015 AU - Bodoni, Aline Faccioli AU - Coeli-Lacchini, Fernanda Borchers AU - Souza, Jorge Estefano de AU - Moreira, Ayrton Custódio AU - Elias, Lucila Leico Kagohara AU - Silva Júnior, Wilson Araújo da AU - Castro, Margaret de AU - Antonini, Sonir Roberto Rauber T2 - Congresso Paulista de Endocrinologia e Metabologia - COPEM J2 - Resumos PP - São Paulo PB - SBEM ER -