Evaluation of mutations in the isocitrate dehydrogenase genes in therapy-related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy
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| Description | article |
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author: Alexander Deutsch Heinz Sill |
| Publication date | January 20, 2011 |
| Language | English |
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