A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies
Ernest Turro, Daniel Greene, Anouck Wijgaerts, Chantal Thys, Claire Lentaigne, Tadbir K Bariana, Sarah K Westbury, Anne M Kelly, Dominik Selleslag, Jonathan C Stephens, Sofia Papadia, Ilenia Simeoni, Christopher J Penkett, Sofie Ashford, Antony Attwood, Steve Austin, Tamam Bakchoul, Peter Collins, Sri V V Deevi, Rémi FavierMyrto Kostadima, Michele P Lambert, Mary Mathias, Carolyn M Millar, Kathelijne Peerlinck, David J Perry, Sol Schulman, Deborah Whitehorn, Christine Wittevrongel, BRIDGE-BPD Consortium, Marc De Maeyer, Augusto Rendon, Keith Gomez, Wendy N Erber, Andrew D Mumford, Paquita Nurden, Kathleen Stirrups, John R Bradley, F Lucy Raymond, Michael A Laffan, Chris Van Geet, Sylvia Richardson, Kathleen Freson, Willem H Ouwehand
Research output: Contribution to journal › Article (Academic Journal) › peer-review
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