Congenital disorder of deglycosilation: clinical phenotype and cell morphology (2016)
Source: Abstracts. Conference titles: Brazilian-International Congress of Genetics. Unidade: FMRP
Subjects: NEUROGENÉTICA, RETÍCULO ENDOPLASMÁTICO
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QUARESEMIN, N. R. et al. Congenital disorder of deglycosilation: clinical phenotype and cell morphology. 2016, Anais.. Caxambu: SBG, 2016. . Acesso em: 26 jan. 2026.APA
Quaresemin, N. R., Diniz, G. M. M., Lourenço, C. M., Gomes, F. G. F. L. R., Cardoso, J. L. S., Coelho, A. C., et al. (2016). Congenital disorder of deglycosilation: clinical phenotype and cell morphology. In Abstracts. Caxambu: SBG.NLM
Quaresemin NR, Diniz GMM, Lourenço CM, Gomes FGFLR, Cardoso JLS, Coelho AC, Oliver C, Jamur MC, Fontes AM. Congenital disorder of deglycosilation: clinical phenotype and cell morphology. Abstracts. 2016 ;[citado 2026 jan. 26 ]Vancouver
Quaresemin NR, Diniz GMM, Lourenço CM, Gomes FGFLR, Cardoso JLS, Coelho AC, Oliver C, Jamur MC, Fontes AM. Congenital disorder of deglycosilation: clinical phenotype and cell morphology. Abstracts. 2016 ;[citado 2026 jan. 26 ]
