GFI1B mutations define an emerging form of inherited thrombocytopenia: insights from a case report and literature review
Abstract Inherited thrombocytopenias (ITs) constitute a heterogeneous group of congenital bleeding disorders caused by defects in over 50 genes that predominantly affect platelet production. GFI1B has recently emerged as a critical transcriptional regulator of megakaryocyte and erythroid differentia...
Furkejuvvon:
| Váldodahkkit: | , , , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Springer
2026-03-01
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| Ráidu: | Annals of Hematology |
| Fáttát: | |
| Liŋkkat: | https://doi.org/10.1007/s00277-026-06921-5 |
| Fáddágilkorat: |
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