A missense mutation is associated with the regulatory complement protein factor H deficiency in a patient with concomitant lack of complement component C9 (2007)
- Authors:
- Autor USP: ISAAC, LOURDES - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Publisher: Sociedade Brasileira de Imunologia
- Publisher place: Rio de Janeiro
- Date published: 2007
- Source:
- Título do periódico: Abstracts
- Conference titles: International Congress of Immunology
-
ABNT
FALCÃO, D. A. et al. A missense mutation is associated with the regulatory complement protein factor H deficiency in a patient with concomitant lack of complement component C9. 2007, Anais.. Rio de Janeiro: Sociedade Brasileira de Imunologia, 2007. . Acesso em: 05 maio 2024. -
APA
Falcão, D. A., Reis, E. S., Amano, M. T., Paixão-Cavalcante, D., Florido, M. P. C., Moraes-Vasconcelos, D., et al. (2007). A missense mutation is associated with the regulatory complement protein factor H deficiency in a patient with concomitant lack of complement component C9. In Abstracts. Rio de Janeiro: Sociedade Brasileira de Imunologia. -
NLM
Falcão DA, Reis ES, Amano MT, Paixão-Cavalcante D, Florido MPC, Moraes-Vasconcelos D, Grumach AS, Isaac L. A missense mutation is associated with the regulatory complement protein factor H deficiency in a patient with concomitant lack of complement component C9. Abstracts. 2007 ;[citado 2024 maio 05 ] -
Vancouver
Falcão DA, Reis ES, Amano MT, Paixão-Cavalcante D, Florido MPC, Moraes-Vasconcelos D, Grumach AS, Isaac L. A missense mutation is associated with the regulatory complement protein factor H deficiency in a patient with concomitant lack of complement component C9. Abstracts. 2007 ;[citado 2024 maio 05 ] - Ultrastructural aspects of alpha - 2 - macroglobulin activited mouse macrophages
- Thioester bond plays a role in the human complement component c4 alpha chain cleavage by activated c1s
- A hereditary human complement C3 deficiency due reduced C3 mRNA
- Molecular caracterization of factor I deficency in two brazilian sisters
- Deficiency of factor I is present in two sisters from a family with low levels of factor H
- Parcial analysis of factor I gene in two deficient sisters of this protein
- Um novo caso de deficiência de C3 do sistema complemento humano
- Immunological characterization of a human C3 deficiency
- Inherited complete factor I deficiency associated with systemic lupus enythematosus, higher susceptibility to infection and low levels of factor H
- Concentrations of regulatory complement proteins in Brazilian Nealthy children and adults
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas