Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant disease

Leukemia

Volumn 28, Issue 1, 2014, Pages 129-137

  Kohlmann, A ^a   Nadarajah, N ^a   Alpermann, T ^a   Grossmann, V ^a   Schindela, S ^a   Dicker, F ^a   Roller, A ^a   Kern, W ^a   Haferlach, C ^a   Schnittger, S ^a   Haferlach, T ^a  

^a MLL MUNICH LEUKEMIA LABORATORY   (Germany)

Author keywords

mutation analysis; next generation sequencing; RUNX1

Indexed keywords

TRANSCRIPTION FACTOR RUNX1;

ACUTE GRANULOCYTIC LEUKEMIA; ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; EVENT FREE SURVIVAL; FEMALE; GENE MUTATION; GENE SEQUENCE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MIDDLE AGED; MINIMAL RESIDUAL DISEASE; NEWBORN; OVERALL SURVIVAL; PRESCHOOL CHILD; PRIORITY JOURNAL; RELAPSE; REMISSION; SCHOOL CHILD; SURVIVAL RATE; SURVIVAL TIME; VERY ELDERLY; YOUNG ADULT;

COHORT STUDIES; CORE BINDING FACTOR ALPHA 2 SUBUNIT; HUMANS; LEUKEMIA, MYELOID, ACUTE; MUTATION;

EID: 84891855434     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/leu.2013.239     Document Type: Article

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