A new activation induced cytidine deaminase (AID) mutation in a brazilian family (2008)
- Authors:
- USP affiliated authors: JACOB, CRISTINA MIUKI ABE - FM ; SAMPAIO, MAGDA MARIA SALES CARNEIRO - FM
- Unidade: FM
- Subjects: DOENÇAS GENÉTICAS; MUTAÇÃO GENÉTICA; BRASILEIROS; ESTUDO DE CASO; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical and Experimental Immunology
- Volume/Número/Paginação/Ano: v. 154, suppl. 1, p. 82, res. P110, 2008
- Conference titles: Meeting of The European Society for Immunodeficiency
-
ABNT
CARNEIRO-SAMPAIO, M. et al. A new activation induced cytidine deaminase (AID) mutation in a brazilian family. Clinical and Experimental Immunology. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 10 out. 2024. , 2008 -
APA
Carneiro-Sampaio, M., Jacob, C. M. A., Reis, P. H., Caratão, N., Barreto, V., & Pastorino, A. C. (2008). A new activation induced cytidine deaminase (AID) mutation in a brazilian family. Clinical and Experimental Immunology. London: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Carneiro-Sampaio M, Jacob CMA, Reis PH, Caratão N, Barreto V, Pastorino AC. A new activation induced cytidine deaminase (AID) mutation in a brazilian family. Clinical and Experimental Immunology. 2008 ; 154 82.[citado 2024 out. 10 ] -
Vancouver
Carneiro-Sampaio M, Jacob CMA, Reis PH, Caratão N, Barreto V, Pastorino AC. A new activation induced cytidine deaminase (AID) mutation in a brazilian family. Clinical and Experimental Immunology. 2008 ; 154 82.[citado 2024 out. 10 ] - Laboratory and clinical description of DiGeorge syndrome patients followed at a reference center: preliminary data
- Follow up of hepatic abscess in chronic granulomatous disease (CGD): clinical experience of a brazilian reference center in primary immunodeficiency (PID)
- Allogeneic hematopoietic stem cell transplantation in children with primary immunodeficiencies: Hospital Israelita Albert Einstein experience
- Chédiak-Higashi syndrome: Experience from a brazilian reference center for primary immunodeficiency
- Autoimunidade em pacientes com síndrome de Down
- Transient hypogamaglobulinemia of infancy: a review of clinical findings and evolution of patients
- Hemophagocytic syndrome associated to NK cells deficiency: a case report
- Restricted T-cell repertoire in four immunodysregulation polyendocrinopathy X-linked (IPEX) infants
- Chronic mucocutaneous candidiasis and its different faces
- Avaliação da função tímica em pacientes com síndrome de DiGeorge
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
