Rapid detection of DNMT3A R882 codon mutations allows early identification of poor risk patients with acute myeloid leukemia
Author:
Publisher
Informa UK Limited
Subject
Cancer Research,Oncology,Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10428194.2012.736986
Reference15 articles.
1. DNMT3AMutations in Acute Myeloid Leukemia
2. Array-based genomic resequencing of human leukemia
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4. Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia
5. Prognostic significance of DNA methyltransferase 3A mutations in cytogenetically normal acute myeloid leukemia: a study by the Acute Leukemia French Association
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