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• W2793167060 abstract "Key Points A single rare DNMT3A mutation and recurrent amplification of ETS1, PTPN6, and TGFBR2 are identified in iMCD and UCD. Genetic alterations in oncogenes, tumor suppressors, and chromatin-remodeling genes are seen in FDCS." @default.
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• W2793167060 date "2018-03-01" @default.
• W2793167060 modified "2023-10-17" @default.
• W2793167060 title "Next-generation sequencing of idiopathic multicentric and unicentric Castleman disease and follicular dendritic cell sarcomas" @default.
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• W2793167060 doi "https://doi.org/10.1182/bloodadvances.2017009654" @default.
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