- Title
- 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
- Creators
- Valeria Visconte - Cleveland ClinicAli Tabarroki - Cleveland ClinicHeesun J. Rogers - Cleveland ClinicEdy Hasrouni - Cleveland ClinicFabiola Traina - Universidade Estadual de Campinas (UNICAMP)Hideki Makishima - Cleveland ClinicBetty K. Hamilton - Cleveland ClinicYang Liu - Cleveland ClinicChristine O’Keefe - Universidade Estadual de Campinas (UNICAMP)Alan Lichtin - Cleveland ClinicLeonard Horwitz - Cleveland ClinicMikkael A. Sekeres - Cleveland ClinicFred H. Hsieh - Cleveland ClinicRamon V. Tiu - Cleveland Clinic
- Publication Details
- Haematologica (Roma), Vol.98(9), pp.e105-e107
- Publisher
- Ferrata Storti Foundation
- Academic Unit
- Miller School of Medicine; UMMG Dept of Medicine - Hematology/Oncology
- Language
- English
- Resource Type
- Journal article
- PMID
- 23831919
- PMCID
- PMC3762110
- Record Identifier
- 991031757828602976
Journal article
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 (Roma), Vol.98(9), pp.e105-e107
2013-09-01
PMCID: PMC3762110
PMID: 23831919
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InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.103 Blood Disorders
- 1.103.155 Acute Myeloid Leukemia
- Web Of Science research areas
- Hematology
- ESI research areas
- Clinical Medicine
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Source: InCites