DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia. [electronic resource]
Producer: 20120227Description: 413-4 p. digitalISSN:- 1365-2141
- Acute Disease
- Adolescent
- Age of Onset
- Bone Marrow Cells -- metabolism
- Child
- Child, Preschool
- DNA (Cytosine-5-)-Methyltransferases -- genetics
- DNA Methyltransferase 3A
- Exons -- genetics
- Female
- Humans
- Infant
- Infant, Newborn
- Japan -- epidemiology
- Leukemia, Myeloid -- epidemiology
- Leukemia, Myelomonocytic, Juvenile -- epidemiology
- Male
- Myelodysplastic Syndromes -- epidemiology
- Neoplasms, Second Primary -- epidemiology
- Nuclear Proteins -- genetics
- Nucleophosmin
- RNA, Messenger -- genetics
- RNA, Neoplasm -- genetics
- fms-Like Tyrosine Kinase 3 -- genetics
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Publication Type: Letter; Research Support, Non-U.S. Gov't
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