Familial Polycythemia Caused by a Novel Mutation in the Beta Globin Gene: Essential Role of P50 in Evaluation of Familial Polycythemia

Lignende værker

• Is congenital secondary erythrocytosis/polycythemia caused by activating mutations within the HIF-2α iron-responsive element?
  af: Percy, Melanie J., et al.
  Udgivet: (2007)
• Optimal therapy for polycythemia vera and essential thrombocythemia can only be determined by the completion of randomized clinical trials
  af: Mascarenhas, John, et al.
  Udgivet: (2014)
• Erythropoiesis in Polycythemia Vera is Hyper-Proliferative and has Accelerated Maturation
  af: Bruchova, Hana, et al.
  Udgivet: (2009)
• The Regulated Expression of miRNAs in Normal and Polycythemia Vera Erythropoiesis
  af: Bruchova, Hana, et al.
  Udgivet: (2007)
• Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemia.
  af: Kralovics, R, et al.
  Udgivet: (1998)