Congenital disorder of deglycosilation: clinical phenotype and cell morphology (2016)
- Authors:
- USP affiliated authors: OLIVER, CONSTANCE - FMRP ; JAMUR, MARIA CELIA - FMRP ; FONTES, APARECIDA MARIA - FMRP
- Unidade: FMRP
- Subjects: NEUROGENÉTICA; RETÍCULO ENDOPLASMÁTICO
- Keywords: NGLY1; Endoplasmic reticulum-associated degradation; Neurogenetics; Deglycosylation; Cell morphology
- Language: Inglês
- Imprenta:
- ISBN: 9788589109062
- Source:
- Título do periódico: Abstracts
- Conference titles: Brazilian-International Congress of Genetics
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ABNT
QUARESEMIN, N. R. et al. Congenital disorder of deglycosilation: clinical phenotype and cell morphology. 2016, Anais.. Caxambu: SBG, 2016. . Acesso em: 16 abr. 2024. -
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 2024 abr. 16 ] -
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 2024 abr. 16 ] - Interaction between LYN and derivates of the ganglioside GD is essential for mast cell activation via FerRI
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