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. 2023 Sep;202(5):e36-e38.
doi: 10.1111/bjh.18935. Epub 2023 Jun 12.

Mitochondria retention in mature RBCs from haemoglobin SC patients

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Mitochondria retention in mature RBCs from haemoglobin SC patients

Sofia Esperti et al. Br J Haematol. 2023 Sep.
No abstract available

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References

REFERENCES

    1. Hannemann A, Weiss E, Rees DC, Dalibalta S, Ellory JC, Gibson JS. The properties of red blood cells from patients heterozygous for HbS and HbC (HbSC genotype). Anemia. 2011;2011:248527.
    1. Hofrichter J, Ross PD, Eaton WA. Kinetics and mechanism of deoxyhemoglobin S gelation: a new approach to understanding sickle cell disease. Proc Natl Acad Sci U S A. 1974;71:4864-8.
    1. Huisman TH, Schroeder WA, Bouver NG, Miller A, Shelton JR, Shelton JB, et al. Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants. Clin Chim Acta. 1972;38:5-16.
    1. Hirsch RE, Raventos-Suarez C, Olson JA, Nagel RL. Ligand state of intraerythrocytic circulating HbC crystals in homozygote CC patients. Blood. 1985;66:775-7.
    1. Nagel RL, Fabry ME, Steinberg MH. The paradox of hemoglobin SC disease. Blood Rev. 2003;17:167-78.

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