Humoral deficiency in a novel GATA2 mutation: anew clinical presentation successfully treated with hematopoietic stem cell transplantation (2020)
- Authors:
- Autor USP: CONDINO NETO, ANTONIO - ICB
- Unidade: ICB
- DOI: 10.1002/pbc.28374
- Subjects: IMUNOLOGIA; CÉLULAS-TRONCO; HEMATOPOESE; MUTAÇÃO GENÉTICA; IMUNOLOGIA DE TRANSPLANTES
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Pediatric Blood & Cancer
- ISSN: 1545-5017
- Volume/Número/Paginação/Ano: v. 67, n. 9, art. e28374, 2 p., 2020
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
PORTICH, Júlia Plentz e CONDINO NETO, Antonio e FAULHABER, Gustavo Adolpho Moreira. Humoral deficiency in a novel GATA2 mutation: anew clinical presentation successfully treated with hematopoietic stem cell transplantation. Pediatric Blood & Cancer. Hoboken: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/pbc.28374. Acesso em: 19 abr. 2024. , 2020 -
APA
Portich, J. P., Condino Neto, A., & Faulhaber, G. A. M. (2020). Humoral deficiency in a novel GATA2 mutation: anew clinical presentation successfully treated with hematopoietic stem cell transplantation. Pediatric Blood & Cancer. Hoboken: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.1002/pbc.28374 -
NLM
Portich JP, Condino Neto A, Faulhaber GAM. Humoral deficiency in a novel GATA2 mutation: anew clinical presentation successfully treated with hematopoietic stem cell transplantation [Internet]. Pediatric Blood & Cancer. 2020 ; 67( 9): 2 .[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/pbc.28374 -
Vancouver
Portich JP, Condino Neto A, Faulhaber GAM. Humoral deficiency in a novel GATA2 mutation: anew clinical presentation successfully treated with hematopoietic stem cell transplantation [Internet]. Pediatric Blood & Cancer. 2020 ; 67( 9): 2 .[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/pbc.28374 - Anhidrotic ectodermal dysplasia and T cell immunodeficiency
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Informações sobre o DOI: 10.1002/pbc.28374 (Fonte: oaDOI API)
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