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2. Caspase-3 is involved in the signalling in erythroid differentiation by targeting late progenitors.

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3. Alterations of red blood cell metabolome in overhydrated hereditary stomatocytosis

4. Bio-engineered and native red blood cells from cord blood exhibit the same metabolomic profile

5. Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K–dependent coagulation factor deficiency

6. Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolome

7. Compound Heterozygosity of a W493C Substitution and R704/Premature Stop Codon within the γ-Glutamyl Carboxylase in Combined Vitamin K-Dependent Coagulation Factor Deficiency in a French Family

8. Compound Heterozygosity in the Novel Mutations W157R and T591K in the γ-Glutamyl Carboxylase Gene Causes Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency in a Tunisian Family