Impact of <scp><i>ASXL1</i></scp> Gene Alterations on Myelodysplastic Syndrome With Isolated 20q Deletion
ASXL1 mutations are one of the late genetic events in MDS patients with isolated 20q deletion, and different types of ASXL1 gene alterations have distinct clinical and biological characteristics.
Authors
- Chengwen Li (ORCID: https://orcid.org/0000-0003-4397-4561)
- Zhijian Xiao (ORCID: https://orcid.org/0000-0001-8008-7385)
- Jiange He
- Linlin Liu (ORCID: https://orcid.org/0009-0007-1044-5897)
- Zefeng Xu (ORCID: https://orcid.org/0009-0001-0147-2291)
- Huijun Wang (ORCID: https://orcid.org/0000-0001-6319-498X)
- Ji Zhou (ORCID: https://orcid.org/0009-0003-3429-9979)
- Ruixue Zhang (ORCID: https://orcid.org/0000-0002-9418-8125)
- W.J. Wu (ORCID: https://orcid.org/0009-0002-7592-9140)
- Yanan Chang (ORCID: https://orcid.org/0000-0002-5466-9397)
- Qi Sun (ORCID: https://orcid.org/0000-0001-5576-580X)
- Yujiao Jia (ORCID: https://orcid.org/0009-0000-5751-9151)
- Tiejun Qin
- Jigang Xiao
- Chenghua Cui
Institutions
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Peking University (CN)
- Peking University People's Hospital (CN)
- Second Hospital of Tianjin Medical University (CN)
- Institute of Hematology & Blood Diseases Hospital (CN)
- Tianjin Medical University (CN)
Publication Details
- Journal
- Cancer Medicine
- Published
- 2025-03-01
- DOI
- https://doi.org/10.1002/cam4.70747
- Primary Topic
- Acute Myeloid Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China