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KMT2A Partial Tandem Duplications (KMT2A-PTD) Is a Rare, but Recurrent Genomic Event in Childhood AML and Associated with High Rate of Co-Occurring FLT3 Mutations

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Year: 2021
Type: conference-abstract
Source: Blood
DOI: 10.1182/blood-2021-147565
Authors: Danielle C. Kirkey, Katherine Tarlock, Rhonda E. Ries, Yi-Cheng Wang, Amanda R. Leonti, Quy Le, Jenny L. Smith, Leila Robinson, Yanling Liu, Quang Tran, Richard Aplenc, Jessica A. Pollard, Anders E. Kolb, Todd A. Alonzo, Xiaotu Ma, Soheil Meshinchi
Institutions: Seattle Children's Hospital, Fred Hutch Cancer Center, Children's Oncology Group, St. Jude Children's Research Hospital, Children's Hospital of Philadelphia, Harvard University, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Alfred I. duPont Hospital for Children, University of Southern California
Language: English

Topic: Acute Myeloid Leukemia Research
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W3212611534
Cites:
Cited by: 3
Related to: 10
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