Source: Resumos. Conference titles: Congresso Paulista de Endocrinologia e Metabologia - COPEM. Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, ENDOCRINOLOGIA
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BODONI, Aline Faccioli et al. Whole exome sequencing identifies a homozygous mutation in nicotinamide nucleotide transidrogenase as the cause of familial glucocorticoid deficiency. 2015, Anais.. São Paulo: SBEM, 2015. . Acesso em: 14 nov. 2024.APA
Bodoni, A. F., Coeli-Lacchini, F. B., Souza, J. E. de, Moreira, A. C., Elias, L. L. K., Silva Júnior, W. A. da, et al. (2015). Whole exome sequencing identifies a homozygous mutation in nicotinamide nucleotide transidrogenase as the cause of familial glucocorticoid deficiency. In Resumos. São Paulo: SBEM.NLM
Bodoni AF, Coeli-Lacchini FB, Souza JE de, Moreira AC, Elias LLK, Silva Júnior WA da, Castro M de, Antonini SRR. Whole exome sequencing identifies a homozygous mutation in nicotinamide nucleotide transidrogenase as the cause of familial glucocorticoid deficiency. Resumos. 2015 ;[citado 2024 nov. 14 ]Vancouver
Bodoni AF, Coeli-Lacchini FB, Souza JE de, Moreira AC, Elias LLK, Silva Júnior WA da, Castro M de, Antonini SRR. Whole exome sequencing identifies a homozygous mutation in nicotinamide nucleotide transidrogenase as the cause of familial glucocorticoid deficiency. Resumos. 2015 ;[citado 2024 nov. 14 ]
