SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype (2013)
- Authors:
- Autor USP: TRAINA, FABÍOLA - FMRP
- Unidade: FMRP
- DOI: 10.3324/haematol.2013.090506
- Subjects: HEMATOLOGIA; CÉLULAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Haematologica
- ISSN: 0390-6078
- Volume/Número/Paginação/Ano: v. 98, n. 9, p. e105-e107, 2013
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
VISCONTE, Valeria et al. SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype. Haematologica. Pavia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.3324/haematol.2013.090506. Acesso em: 06 fev. 2026. , 2013 -
APA
Visconte, V., Tabarroki, A., Rogers, H. J., Hasrouni, E., Traina, F., Makishima, H., et al. (2013). SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype. Haematologica. Pavia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.3324/haematol.2013.090506 -
NLM
Visconte V, Tabarroki A, Rogers HJ, Hasrouni E, Traina F, Makishima H, Hamilton BK, Liu Y, O'Keefe C, Lichtin A, Horwitz L, Sekeres MA, Hsieh FH, Tiu RV. SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype [Internet]. Haematologica. 2013 ; 98( 9): e105-e107.[citado 2026 fev. 06 ] Available from: https://doi.org/10.3324/haematol.2013.090506 -
Vancouver
Visconte V, Tabarroki A, Rogers HJ, Hasrouni E, Traina F, Makishima H, Hamilton BK, Liu Y, O'Keefe C, Lichtin A, Horwitz L, Sekeres MA, Hsieh FH, Tiu RV. SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype [Internet]. Haematologica. 2013 ; 98( 9): e105-e107.[citado 2026 fev. 06 ] Available from: https://doi.org/10.3324/haematol.2013.090506 - Familial systemic mastocytosis with germline KIT K509I mutation is sensitive to treatment with imatinib, dasatinib and PKC412
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Informações sobre o DOI: 10.3324/haematol.2013.090506 (Fonte: oaDOI API)
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