SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors (2019)
- Authors:
- USP affiliated authors: KRIEGER, JOSE EDUARDO - FM ; SABINO, ESTER CERDEIRA - FM ; ROCHA, VANDERSON GERALDO - FM
- Unidade: FM
- DOI: 10.1016/j.bcmd.2019.03.006
- Subjects: DOADORES DE SANGUE; EXPRESSÃO GÊNICA; ANTÍGENOS; GRUPOS SANGUÍNEOS; REAÇÃO TRANSFUSIONAL; BRASIL
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Blood cells molecules and diseases
- ISSN: 1079-9796
- Volume/Número/Paginação/Ano: v. 77, p. 23-28, 2019
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
DEZAN, Marcia Regina et al. SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors. Blood cells molecules and diseases, v. 77, p. 23-28, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2019.03.006. Acesso em: 03 jan. 2026. -
APA
Dezan, M. R., Costa-neto, A., Gomes, C. N., Ribeiro, I. H., Oliveira, V. B., V, M. C. A. C., et al. (2019). SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors. Blood cells molecules and diseases, 77, 23-28. doi:10.1016/j.bcmd.2019.03.006 -
NLM
Dezan MR, Costa-neto A, Gomes CN, Ribeiro IH, Oliveira VB, V MCAC, Oliveira TGM, Krieger JE, Sabino EC, Rocha VG. SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors [Internet]. Blood cells molecules and diseases. 2019 ; 77 23-28.[citado 2026 jan. 03 ] Available from: https://doi.org/10.1016/j.bcmd.2019.03.006 -
Vancouver
Dezan MR, Costa-neto A, Gomes CN, Ribeiro IH, Oliveira VB, V MCAC, Oliveira TGM, Krieger JE, Sabino EC, Rocha VG. SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors [Internet]. Blood cells molecules and diseases. 2019 ; 77 23-28.[citado 2026 jan. 03 ] Available from: https://doi.org/10.1016/j.bcmd.2019.03.006 - High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype
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Informações sobre o DOI: 10.1016/j.bcmd.2019.03.006 (Fonte: oaDOI API)
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