Platelet CD34 expression and α/δ-granule abnormalities in GFI1B - and RUNX1 -related familial bleeding disorders
2017
To the editor:
Mutations in the transcription factor Growth Factor Independent 1B ( GFI1B ) are causal to an autosomal dominant inherited bleeding disorder characterized by macrothrombocytopenia and reduced platelet α-granule numbers (platelet-type bleeding disorder-17, Online Mendelian
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