Open AccessSF3B1 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
Author(s) -
Valeria Visconte,
Ali Tabarroki,
Heesun J. Rogers,
Edy Hasrouni,
Fabı́ola Traina,
Hideki Makishima,
Betty K. Hamilton,
Yang Liu,
Christine L. O’Keefe,
Alan E. Lichtin,
Leonard Horwitz,
Mikkael A. Sekeres,
Fred H. Hsieh,
Ramon V. Tiu
Publication year - 2013
Publication title -
haematologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.782
H-Index - 142
eISSN - 1592-8721
pISSN - 0390-6078
DOI - 10.3324/haematol.2013.090506
Subject(s) - myelodysplastic syndromes , bone marrow failure , bone marrow , aplastic anemia , phenotype , medicine , peripheral blood , haematopoiesis , immunology , biology , stem cell , gene , genetics