Article

A Novel EPO Gene Mutation In a Family With Autosomal Dominant Polycythemia

2013-11-15

Abstract excerpt

Abstract Familial polycythemia/erythrocytosis (ECYT by OMIM), characterized by an absolute increase in red cell mass, is a heterogeneous group of disorders that can be attributed to either intrinsic erythroid progenitor defects, resulting in their hyperproliferation (primary polycythemias), or from circulating extracellular factors such as erythropoietin (EPO) stimulating erythropoiesis (secondary polycythemias)....

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Literature Corpus work: feea0321-193b-52c4-b224-8c576a5ed958
DOI: 10.1182/blood.v122.21.950.950

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