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Volumn 98, Issue 11, 2013, Pages 1689-1696

Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRD2 GENE; CAP2 GENE; CARD6 GENE; CASE REPORT; CHROMOSOME ANALYSIS; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; GRANULOCYTE; HUMAN; HUMAN CELL; HUMAN TISSUE; KIAA0355 GENE; MALE; MFRP GENE; MYELOFIBROSIS; NONSENSE MUTATION; POINT MUTATION; POLYCYTHEMIA; POLYMERASE CHAIN REACTION; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS; SKIN FIBROBLAST; SOMATIC MUTATION; SOX30 GENE; THROMBOCYTHEMIA;

EID: 84887004529     PISSN: 03906078     EISSN: 15928721     Source Type: Journal    
DOI: 10.3324/haematol.2013.092379     Document Type: Article
Times cited : (9)

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