Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopeniaIrina Pleines(The University of Melbourne), Benjamin T. Kile(Discovery Institute)Journal of Clinical InvestigationJanuary 29, 201710.1172/jci86154Cited by 80SaveCiteExport RISWatch citationsRelated PapersMegakaryocyte-specific RhoA deficiency causes macrothrombocytopenia and defective platelet activation in hemostasis and thrombosis|Blood|2011|174Cell death following the loss of ADAR1 mediated A-to-I RNA editing is not effected by the intrinsic apoptosis pathway|Cell Death and Disease|2019|15