IDH1 and IDH2 mutations in therapy-related myelodysplastic syndrome and acute myeloid leukemia are associated with a normal karyotype and with der(1;7)(q10;p10)

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Bibliographische Detailangaben
Veröffentlicht in:	Leukemia 2013-04, Vol.27 (4), p.957-959
Hauptverfasser:	Westman, M K, Pedersen-Bjergaard, J, Andersen, M T, Andersen, M K
Format:	Artikel
Sprache:	eng
Schlagworte:	692/420/2489/68 692/420/755 692/699/67/1990/1673 692/699/67/1990/283/1897 Acute myeloid leukemia Adult Aged Cancer Cancer Research Care and treatment Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 7 Critical Care Medicine Dehydrogenases Epigenetics Female Gene mutations Genetic aspects Hematology Humans Intensive Internal Medicine Isocitrate Dehydrogenase - genetics Karyotypes Karyotyping letter-to-the-editor Letters to the editor Leukemia Leukemia, Myeloid, Acute - genetics Male Medicine Medicine & Public Health Middle Aged Multiple myeloma Mutation Myelodysplastic syndrome Myelodysplastic syndromes Myelodysplastic Syndromes - chemically induced Myelodysplastic Syndromes - genetics Oncology Physiological aspects Radiation therapy Transcription factors Translocation, Genetic
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