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Volumn 29, Issue 3, 2015, Pages 660-667

WT1 mutations are secondary events in AML, show varying frequencies and impact on prognosis between genetic subgroups

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADOLESCENT; ADULT; ADVERSE OUTCOME; AGE; AGED; ARTICLE; CANCER PATIENT; CANCER PROGNOSIS; CANCER SURVIVAL; CEBPA GENE; CLINICAL ARTICLE; COHORT ANALYSIS; DNMT3A GENE; EVENT FREE SURVIVAL; EXON; FEMALE; FLT3 GENE; FRAMESHIFT MUTATION; GENE DUPLICATION; GENE FREQUENCY; GENE MUTATION; GENETIC VARIABILITY; HUMAN; IDH1 GENE; IDH2 GENE; INCIDENCE; INDEL MUTATION; KARYOTYPE; MALE; MISSENSE MUTATION; MUTATION RATE; MUTATIONAL ANALYSIS; MUTATOR GENE; NONSENSE MUTATION; PML RARA GENE; PRIORITY JOURNAL; SEX DIFFERENCE; SPLICE SITE MUTATION; TUMOR GENE; WILMS TUMOR 1 GENE; GENE EXPRESSION REGULATION; GENETICS; LEUKEMIA, MYELOID, ACUTE; MIDDLE AGED; MORTALITY; MUTATION; NERVE FIBER; PATHOLOGY; PROGNOSIS; SURVIVAL; VERY ELDERLY;

EID: 84924532448     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/leu.2014.243     Document Type: Article
Times cited : (59)

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