Molecular characterisation of human complement factor I deficiencies in two Brazilian families (2008)
- Authors:
- USP affiliated authors: CONDINO NETO, ANTONIO - ICB ; ISAAC, LOURDES - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Molecular Immunology
- Volume/Número/Paginação/Ano: v. 45, n. 16, 2008
- Conference titles: International Complement Workshop
-
ABNT
DELCOLLI, Maria Isabel et al. Molecular characterisation of human complement factor I deficiencies in two Brazilian families. Molecular Immunology. Chicago: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 10 jan. 2026. , 2008 -
APA
Delcolli, M. I., Rodrigues, V. H., Silva, C., Reis, E., Florido, M., Nudelman, V., et al. (2008). Molecular characterisation of human complement factor I deficiencies in two Brazilian families. Molecular Immunology. Chicago: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Delcolli MI, Rodrigues VH, Silva C, Reis E, Florido M, Nudelman V, Leitão M, Condino Neto A, Isaac L. Molecular characterisation of human complement factor I deficiencies in two Brazilian families. Molecular Immunology. 2008 ; 45( 16):[citado 2026 jan. 10 ] -
Vancouver
Delcolli MI, Rodrigues VH, Silva C, Reis E, Florido M, Nudelman V, Leitão M, Condino Neto A, Isaac L. Molecular characterisation of human complement factor I deficiencies in two Brazilian families. Molecular Immunology. 2008 ; 45( 16):[citado 2026 jan. 10 ] - Caracterização molecular das deficiências no componente fator I do complemento humano em duas famílias brasileiras
- Molecular characterization of human complement factor I in two brazilian families
- Ligação de leptospira interrogans serovar pomona às diferentes variantes de fator H (TYR402 and HIS402)
- Intravitreal levels of human complement factor F (CFH) in patients with exudative age-related macular degeneration (AMD)
- Associação entre polimorfismo de fator H (Y402H) e degeneração da mácula relacionada à idade
- Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians
- ARG 127 his substitution in SCR-2 of the regulatory complement protein factor H is found in a factor H deficient patient with concomitant lack of complement component C9
- Characterization and genetic analysis of human complement Factor I deficiency
- Immunological and genetic characterization of deficiency of the component C5 of the human complement system
- Human complement factor H (Y402H) polymorphism and age-related macular degeneration (AMD) in brazilian patients
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