P1436: DEVELOPMENT OF A BETA-GLOBIN GENE REPLACEMENT STRATEGY AS A THERAPEUTIC APPROACH FOR ΒETA-THALASSEMIA

Antzeko izenburuak

• PB2532: VARIABLE HEMATOLOGICAL AND CLINICAL PHENOTYPES IN DOUBLE HETEROZYGOTES OF ΒETA-THALASSEMIA AND TRIPLICATED ΑLPHA-GLOBIN GENES
  nork: Polyxeni Delaporta, et al.
  Argitaratua: (2023-08-01)
• Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia
  nork: Maria Carla Sollaino, et al.
  Argitaratua: (2009-10-01)
• PB2237: HEMATIMETRIC DETECTION OF THE TRIPLICATION OF ALPHA-GLOBIN GENES. THE IMPORTANCE OF YOUR DIAGNOSIS
  nork: P. Ropero, et al.
  Argitaratua: (2022-06-01)
• P1436: DEVELOPMENT OF A BETA-GLOBIN GENE REPLACEMENT STRATEGY AS A THERAPEUTIC APPROACH FOR ΒETA-THALASSEMIA
  nork: B. Wienert, et al.
  Argitaratua: (2022-06-01)
• Thalassemia major is a severe anemia that requires blood transfusions. In this study, we searched into the hematological and biochemical status of βeta-thalassemia major patients in Koya. Hematological analysis revealed severe anemia in βeta-thalassemia p
  nork: Kochar Kh. Saleh, et al.
  Argitaratua: (2021-10-01)