Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia (2021)
- Authors:
- USP affiliated authors: MARTINS, DIEGO ANTONIO PEREIRA - FMRP ; SILVA, JUAN LUIZ COELHO DA - FMRP ; WEINHÄUSER, ISABEL - FMRP
- Unidade: FMRP
- DOI: 10.1016/j.htct.2020.03.006
- Subjects: POLIMORFISMO; CÉLULAS; ANEMIA
- Keywords: Clinical outcome; Fetal hemoglobin; HBS1L-MYB polymorphisms; Sickle cell anemia
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: São José do Rio Preto
- Date published: 2021
- Source:
- Título: Hematology, Transfusion and Cell Therapy
- ISSN: 2531-1379
- Volume/Número/Paginação/Ano: v. 43, n. 3, p. 243-248, 2021
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by-nc-nd
-
ABNT
PEREIRA-MARTINS, Diego Antonio et al. Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia. Hematology, Transfusion and Cell Therapy, v. 43, n. 3, p. 243-248, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.htct.2020.03.006. Acesso em: 27 dez. 2025. -
APA
Pereira-Martins, D. A., Domingos, I. F., Belini-Junior, E., Coelho-Silva, J. L., Weinhäuser, I., Araújo, A. S., et al. (2021). Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia. Hematology, Transfusion and Cell Therapy, 43( 3), 243-248. doi:10.1016/j.htct.2020.03.006 -
NLM
Pereira-Martins DA, Domingos IF, Belini-Junior E, Coelho-Silva JL, Weinhäuser I, Araújo AS, Lobo CL, Bonini-Domingos CR, Bezerra MA, Lucena-Araujo AR. Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia [Internet]. Hematology, Transfusion and Cell Therapy. 2021 ; 43( 3): 243-248.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1016/j.htct.2020.03.006 -
Vancouver
Pereira-Martins DA, Domingos IF, Belini-Junior E, Coelho-Silva JL, Weinhäuser I, Araújo AS, Lobo CL, Bonini-Domingos CR, Bezerra MA, Lucena-Araujo AR. Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia [Internet]. Hematology, Transfusion and Cell Therapy. 2021 ; 43( 3): 243-248.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1016/j.htct.2020.03.006 - Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort
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Informações sobre o DOI: 10.1016/j.htct.2020.03.006 (Fonte: oaDOI API)
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