Homozygous hereditary C3 deficiency due to a premature stop codon (2002)
- Authors:
- USP affiliated authors: ISAAC, LOURDES - ICB ; FARAH, SHAKER CHUCK - IQ
- Unidades: ICB; IQ
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of Clinical Immunology
- ISSN: 0271-9142
- Volume/Número/Paginação/Ano: v. 22, n. 6, p. 321-330, 2002
-
ABNT
REIS, Edimara da Silva et al. Homozygous hereditary C3 deficiency due to a premature stop codon. Journal of Clinical Immunology, v. 22, n. 6, p. 321-330, 2002Tradução . . Acesso em: 18 out. 2024. -
APA
Reis, E. da S., Baracho, G. V., Lima, A. S., Farah, C. S., & Isaac, L. (2002). Homozygous hereditary C3 deficiency due to a premature stop codon. Journal of Clinical Immunology, 22( 6), 321-330. -
NLM
Reis E da S, Baracho GV, Lima AS, Farah CS, Isaac L. Homozygous hereditary C3 deficiency due to a premature stop codon. Journal of Clinical Immunology. 2002 ; 22( 6): 321-330.[citado 2024 out. 18 ] -
Vancouver
Reis E da S, Baracho GV, Lima AS, Farah CS, Isaac L. Homozygous hereditary C3 deficiency due to a premature stop codon. Journal of Clinical Immunology. 2002 ; 22( 6): 321-330.[citado 2024 out. 18 ] - C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene
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