GATA1 erythroid-specific regulation of SEC23B expression and its implication in the pathogenesis of congenital dyserythropoietic anemia type II

Gelijkaardige items

• Hereditary spherocytosis and allied disorders
  door: Roberta Russo, et al.
  Gepubliceerd in: (2019-06-01)
• Red cells in post-genomic era: impact of personalized medicine in the treatment of anemias
  door: Achille Iolascon, et al.
  Gepubliceerd in: (2015-01-01)
• Next generation research and therapy in red blood cell diseases
  door: Roberta Russo, et al.
  Gepubliceerd in: (2016-05-01)
• PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis
  door: Immacolata Andolfo, et al.
  Gepubliceerd in: (2018-03-01)
• Hereditary anemia caused by multilocus inheritance of <i>PIEZO1</i>, <i>SLC4A1</i> and <i>ABCB6</i> mutations: a diagnostic and therapeutic challenge
  door: Barbara Eleni Rosato, et al.
  Gepubliceerd in: (2022-04-01)