Associated Papers
The congenital dyserythropoieitic anemias: genetics and pathophysiology.
King R et al.
Current Opinion in Hematology, 2022
Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review.
Tangsricharoen T et al.
British Journal of Haematology, 2021
Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review.
Xu L et al.
Frontiers in Genetics, 2021
A Very Rare Congenital Dyserythropoietic Anemia Variant-Type IV in a Patient With a Novel Mutation in the KLF1 Gene: A Case Report and Review of the Literature.
Belgemen-Ozer T et al.
Journal of Pediatric Hematology/oncology, 2020
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