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Volumn 126, Issue 2, 2015, Pages 233-241

SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts

(22)  Malcovati, Luca a,b   Karimi, Mohsen c   Papaemmanuil, Elli d   Ambaglio, Ilaria a,b   Jädersten, Martin c   Jansson, Monika c   Elena, Chiara a,b   Gallì, Anna b   Walldin, Gunilla c   Porta, Matteo G Della a,b   Raaschou Jensen, Klas e   Travaglino, Erica b   Kallenbach, Klaus e   Pietra, Daniela b   Ljungström, Viktor f   Conte, Simona c   Boveri, Emanuela g   Invernizzi, Rosangela a,g   Rosenquist, Richard f   Campbell, Peter J d   more..


Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CHRONIC MYELOMONOCYTIC LEUKEMIA; DISEASE COURSE; DNA METHYLATION; FEMALE; GENE; GENE SEQUENCE; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; MALE; OVERALL SURVIVAL; PHENOTYPE; PRIORITY JOURNAL; REFRACTORY ANEMIA WITH EXCESS BLASTS; REFRACTORY ANEMIA WITH RINGED SIDEROBLASTS; REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA; REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA AND RINGED SIDEROBLASTS; REFRACTORY CYTOPENIA WITH UNILINEAGE DYSPLASIA; SF3B1 GENE; SOMATIC MUTATION; ADOLESCENT; ANEMIA, SIDEROBLASTIC; CLASSIFICATION; DIFFERENTIAL DIAGNOSIS; GENETICS; MIDDLE AGED; MUTATION; MYELODYSPLASTIC SYNDROMES; PROGNOSIS; VERY ELDERLY; YOUNG ADULT;

EID: 84937805127     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2015-03-633537     Document Type: Article
Times cited : (340)

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