Whole exome sequencing identifies a homozygous mutation in nicotinamide nucleotide transidrogenase as the cause of familial glucocorticoid deficiency (2015)
- Autores:
- Autores USP: CASTRO, MARGARET DE - FMRP ; MOREIRA, AYRTON CUSTODIO - FMRP ; ELIAS, LUCILA LEICO KAGOHARA - FMRP ; SILVA JUNIOR, WILSON ARAÚJO DA - FMRP ; ANTONINI, SONIR ROBERTO RAUBER - FMRP
- Unidade: FMRP
- Assuntos: MUTAÇÃO GENÉTICA; ENDOCRINOLOGIA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Resumos
- Nome do evento: Congresso Paulista de Endocrinologia e Metabologia - COPEM
-
ABNT
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: 25 set. 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 set. 25 ] -
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 set. 25 ] - Whole exome: análise exploratória do exoma de um paciente com deficiência familiar de glicocorticoide
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