Anemia‐associated mutations disrupt the CDIN1 ‐Codanin1 complex in inherited congenital dyserythropoietic anemia I ( CDA ‐I) disease

Ähnliche Einträge

• Neonatal diagnosis of congenital dyserythropoietic anemia type II
  von: Apolline Lelard, et al.
  Veröffentlicht: (2024)
• Novel mutation in KIF23 causing congenital dyserythropoietic anemia type III in patients who underwent allogeneic hematopoietic stem cell transplantation
  von: Tomoko Fujikawa, et al.
  Veröffentlicht: (2024)
• Comment on: Severe β‐thalassemia (Hb Zunyi) mimicking congenital dyserythropoietic anemia—The deceivingly normal mean corpuscular volume and hemoglobin electrophoresis in dominantly inherited β‐thalassemia: Hb Little Venice
  von: Anselm Chi‐wai Lee, et al.
  Veröffentlicht: (2024)
• Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias
  von: Roberta Russo, et al.
  Veröffentlicht: (2024)
• Congenital dyserythropoietic anemia type IV with KLF1 E325K mutation: A new case with dysmorphic male genitalia
  von: Gita V. Massey, et al.
  Veröffentlicht: (2024)