Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21).
Overview
publication date
published in
Research
keywords
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Chromosomes, Human, Pair 21
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Chromosomes, Human, Pair 8
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Leukemia, Myeloid, Acute
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Mutation
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Repressor Proteins
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Transcription Factors
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Translocation, Genetic
Identity
Scopus Document Identifier
Digital Object Identifier (DOI)
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10.3109/10428194.2015.1037754
PubMed ID
Additional Document Info
has global citation frequency
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