Pyruvate kinase deficiency misdiagnosed as congenital dyserythropoietic anemia type i

Antzeko izenburuak

• Novel PKLR missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred—PK deficiency masquerading as congenital dyserythropoietic anemia
  nork: Naglaa Fawaz, et al.
  Argitaratua: (2022-02-01)
• Pyruvate kinase deficiency misdiagnosed as congenital dyserythropoietic anemia type i
  nork: A. Koca Yozgat, et al.
  Argitaratua: (2020-10-01)
• Rare congenital Dyserythropoietic anemia of childhood: A case report
  nork: Hamzeh F. Al Hussien, et al.
  Argitaratua: (2023-02-01)
• Congenital dyserythropoietic anemia type IV with kruppel-like factor 1 E325K mutation in a preterm neonate: Case and literature review
  nork: Reema Garegrat, et al.
  Argitaratua: (2022-01-01)
• Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
  nork: Fatih Demircioğlu, et al.
  Argitaratua: (2015-07-01)