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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

Journal of Hematology & Thromboembolic Diseases, Vol: 02, Issue: 06
2014
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Journal of Hematology & Thromboembolic Diseases

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