Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability (2009)
- Authors:
- USP affiliated authors: FARAH, SHAKER CHUCK - IQ ; ISAAC, LOURDES - ICB
- Unidades: IQ; ICB
- DOI: 10.1016/j.molimm.2008.10.035
- Subjects: MENINGITE; IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Molecular Immunology
- ISSN: 0161-5890
- Volume/Número/Paginação/Ano: v. 46, n. 10, p. 2116-2123, 2009
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
AGUILAR-RAMIREZ, Priscilia et al. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability. Molecular Immunology, v. 46, n. 10, p. 2116-2123, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.molimm.2008.10.035. Acesso em: 26 abr. 2024. -
APA
Aguilar-Ramirez, P., Reis, E. da S., Florido, M. P. C., Barbosa, A. S., Farah, C. S., Costa-Carvalho, B. T., & Isaac, L. (2009). Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability. Molecular Immunology, 46( 10), 2116-2123. doi:10.1016/j.molimm.2008.10.035 -
NLM
Aguilar-Ramirez P, Reis E da S, Florido MPC, Barbosa AS, Farah CS, Costa-Carvalho BT, Isaac L. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability [Internet]. Molecular Immunology. 2009 ; 46( 10): 2116-2123.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1016/j.molimm.2008.10.035 -
Vancouver
Aguilar-Ramirez P, Reis E da S, Florido MPC, Barbosa AS, Farah CS, Costa-Carvalho BT, Isaac L. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability [Internet]. Molecular Immunology. 2009 ; 46( 10): 2116-2123.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1016/j.molimm.2008.10.035 - Homozygous hereditary C3 deficiency due to a premature stop codon
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Informações sobre o DOI: 10.1016/j.molimm.2008.10.035 (Fonte: oaDOI API)
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