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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.
- Source :
-
Haematologica [Haematologica] 2013 Sep; Vol. 98 (9), pp. e105-7. Date of Electronic Publication: 2013 Jul 05. - Publication Year :
- 2013
- Subjects :
- Adult
Aged
Anemia, Aplastic
Anemia, Sideroblastic diagnosis
Bone Marrow Diseases
Bone Marrow Failure Disorders
Female
Hemoglobinuria, Paroxysmal diagnosis
Humans
Male
Mastocytosis diagnosis
Phenotype
RNA Splicing Factors
Anemia, Sideroblastic genetics
Hemoglobinuria, Paroxysmal genetics
Mastocytosis genetics
Mutation genetics
Myelodysplastic Syndromes diagnosis
Myelodysplastic Syndromes genetics
Phosphoproteins genetics
Ribonucleoprotein, U2 Small Nuclear genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1592-8721
- Volume :
- 98
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Haematologica
- Publication Type :
- Report
- Accession number :
- 23831919
- Full Text :
- https://doi.org/10.3324/haematol.2013.090506