Case report: Clinical characteristics and genetic analysis of a familial platelet disorder associated with RUNX1 gene mutation
ObjectiveTo explore the clinical and genetic mutation characteristics of familial platelet disorder with acute myeloid leukemia tendency (FPD/AML) caused by RUNX1 germline mutations.MethodsThe clinical data and gene mutation results of a child with FPD/AML and family members admitted to Changzhou Ch...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2025-06-01
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| Series: | Frontiers in Hematology |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/frhem.2025.1608314/full |
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