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MPL gene mutation

Clinical significance: - defects in MPL are a cause of - congenital amegakaryocytic thrombocytopenia - essential thrombocythemia - myelofibrosis

Related

thrombopoietin receptor; TPO-R; myeloproliferative leukemia protein; C-mpl; CD110 (MPL, TPOR)

General

gene mutation testing; gene mutation analysis

References

  1. Medical Knowledge Self Assessment Program (MKSAP) 19 Board Basics. An Enhancement to MKSAP19. American College of Physicians, Philadelphia 2022