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Defective binding of ETS1 and STAT4 due to a mutation in the promoter region of THPO as a novel mechanism of congenital amegakaryocytic thrombocytopenia
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Defective binding of ETS1 and STAT4 due to a mutation in the promoter region of THPO as a novel mechanism of congenital amegakaryocytic thrombocytopenia
Journal
Haematologica-The Hematology Journal
Author(s)
Capaci Valeria
Etai Adam
Ifat Bar-Joseph
Faleschini Michela
Alessandro Pecci
Savoia Anna
DOI
10.3324/haematol.2022.281392
Project(s)
Molecular screening of Inherited Thrombocytopenias and developmental of gene specific functional assays for the characterization of pathogenetic variants: models for the study of THPO, TUBB1, ACTN1 and GFI1B mutations
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