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ERIC 2022 | Identifying low-burden TP53 mutations with NGS in CLL

Florence Cymbalista, MD, Hôpital Avicenne, Bobigny, France, comments on the use of next-generation sequencing (NGS) to identify low-burden TP53 mutations in patients with chronic lymphocytic leukemia (CLL) and use it as a tool for early diagnosis and treatment. This interview took place at the 2022 European Research Initiative on CLL (ERIC) Meeting.

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