RUNX1 Germline Mutation in a Patient with Chronic Thrombocytopenia
One of the pathophysiologic mechanism of inherited thrombocytopenia is a defect in transcription factors that regulate the expression of multiple genes required for megakaryopoiesis. Runt-related transcription factor 1 (RUNX1) binds to its heterodimeric partner, core binding factor beta (CBFβ), and...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
The Korean Society of Pediatric Hematology-Oncology,
2021-10-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |