Fonte: Abstracts. Nome do evento: Congresso Brasileiro de Genética. Unidades: FMRP, FCFRP
Assuntos: HORMÔNIOS GLICOCORTICOIDES, FENÓTIPOS, GENÓTIPOS
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ABNT
BODONI, A. F. et al. Novel mutation P.G866D in NNT gene found in family deficiency glucocorticoids change oxidative state of mononuclear cells. 2015, Anais.. Águas de Lindóia: SBG, 2015. . Acesso em: 15 out. 2024.APA
Bodoni, A. F., Coeli-Lacchini, F. B., Sobral, L. M., Leopoldino, A. M., Moreira, A. C., Elias, L. L. K., et al. (2015). Novel mutation P.G866D in NNT gene found in family deficiency glucocorticoids change oxidative state of mononuclear cells. In Abstracts. Águas de Lindóia: SBG.NLM
Bodoni AF, Coeli-Lacchini FB, Sobral LM, Leopoldino AM, Moreira AC, Elias LLK, Silva Júnior WA da, Castro M de, Antonini SRR. Novel mutation P.G866D in NNT gene found in family deficiency glucocorticoids change oxidative state of mononuclear cells. Abstracts. 2015 ;[citado 2024 out. 15 ]Vancouver
Bodoni AF, Coeli-Lacchini FB, Sobral LM, Leopoldino AM, Moreira AC, Elias LLK, Silva Júnior WA da, Castro M de, Antonini SRR. Novel mutation P.G866D in NNT gene found in family deficiency glucocorticoids change oxidative state of mononuclear cells. Abstracts. 2015 ;[citado 2024 out. 15 ]
