Source: Resumos. Conference titles: Biennial Meenting of the European Society for Immunodeficiencies (ESID). Unidade: ICB
Assunto: IMUNOLOGIA
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ABNT
KLAVER, S. et al. Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients. 2012, Anais.. Florença: The European Society for Immunodeficiencies, 2012. . Acesso em: 11 nov. 2024.APA
Klaver, S., Carvalho, B., Tavares, F., Lima, S., Ferreira, J., Mansur, E., et al. (2012). Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients. In Resumos. Florença: The European Society for Immunodeficiencies.NLM
Klaver S, Carvalho B, Tavares F, Lima S, Ferreira J, Mansur E, Roxo-Junior P, Durandy A, Condino-Neto A. Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients. Resumos. 2012 ;[citado 2024 nov. 11 ]Vancouver
Klaver S, Carvalho B, Tavares F, Lima S, Ferreira J, Mansur E, Roxo-Junior P, Durandy A, Condino-Neto A. Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients. Resumos. 2012 ;[citado 2024 nov. 11 ]
