A novel activation-induced cytidine deaminase (AID) mutation in Brazilian patients with hyper-IgM type 2 syndrome (2013)
- Authors:
- USP affiliated authors: JACOB, CRISTINA MIUKI ABE - FM ; SAMPAIO, MAGDA MARIA SALES CARNEIRO - FM
- Unidade: FM
- DOI: 10.1016/j.clim.2013.05.017
- Subjects: DOENÇAS GENÉTICAS; CRIANÇAS; BRASILEIROS; MUTAÇÃO GENÉTICA; IMUNOGLOBULINAS; SEQUENCIAMENTO GENÉTICO
- Language: Inglês
- Imprenta:
- Source:
- Título: C l i n i c a l Immunology
- ISSN: 1521-6616
- Volume/Número/Paginação/Ano: v. 148, n. 2, p. 279-286, 2013
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by-nc-nd
-
ABNT
CARATÃO, Nadine et al. A novel activation-induced cytidine deaminase (AID) mutation in Brazilian patients with hyper-IgM type 2 syndrome. C l i n i c a l Immunology, v. 148, n. 2, p. 279-286, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.clim.2013.05.017. Acesso em: 30 dez. 2025. -
APA
Caratão, N., Cortesão, C. S., Reis, P. H., Freitas, R. F., Jacob, C. M. A., Pastorino, A. C., et al. (2013). A novel activation-induced cytidine deaminase (AID) mutation in Brazilian patients with hyper-IgM type 2 syndrome. C l i n i c a l Immunology, 148( 2), 279-286. doi:10.1016/j.clim.2013.05.017 -
NLM
Caratão N, Cortesão CS, Reis PH, Freitas RF, Jacob CMA, Pastorino AC, Carneiro-Sampaio M, Barreto VM. A novel activation-induced cytidine deaminase (AID) mutation in Brazilian patients with hyper-IgM type 2 syndrome [Internet]. C l i n i c a l Immunology. 2013 ; 148( 2): 279-286.[citado 2025 dez. 30 ] Available from: https://doi.org/10.1016/j.clim.2013.05.017 -
Vancouver
Caratão N, Cortesão CS, Reis PH, Freitas RF, Jacob CMA, Pastorino AC, Carneiro-Sampaio M, Barreto VM. A novel activation-induced cytidine deaminase (AID) mutation in Brazilian patients with hyper-IgM type 2 syndrome [Internet]. C l i n i c a l Immunology. 2013 ; 148( 2): 279-286.[citado 2025 dez. 30 ] Available from: https://doi.org/10.1016/j.clim.2013.05.017 - Transient hypogamaglobulinemia of infancy: a review of clinical findings and evolution of patients
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Informações sobre o DOI: 10.1016/j.clim.2013.05.017 (Fonte: oaDOI API)
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