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Autosomal Dominant Hereditary Essential Thrombocythemia due to a Gain of Function Mutation in the Thrombopoietin (TPO) and JAK2 Gene as the Cause of Congenital Aspirin-Responsive Sticky Platelet Syndrome: Personal Experiences and Review of the Literature

PICH, Achille;
2014-01-01
2014
02
06
1
8
Autosomal dominant hereditary essential thrombocythemia, Myeloproliferative neoplasm, WHO classification, JAK2 mutation, TPO gene mutation, Myelofibrosis
Jan Jacques Michiels; Jan Stasko; Peter Kubish; Achille Pich; Hendrik De Raeve
03A-Articolo su Rivista
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J Hematol Thromb Dis 2014 Autosomal-dominant-hereditary-essential-thrombocythemia-due-to-a-gain-of-function-mutation-in-the-thrombopoietin-tpo-and-jak-gene-2329-8790.1000180.pdf

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Descrizione: Michiels et al., J Hematol Thromb Dis 2014, 2:6
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1647352
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