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APA Citation
Klei, T. R. L., Kheradmand Kia, S., Veldthuis, M., Dehbozorgian, J., Karimi, M., Geissler, J., Sellink, E., Thiel-Valkhof, M., Burger, P., van Alphen, F., Meijer, A. B., van Bruggen, R., & van Zwieten, R. (2019). a Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia. Hemoglobin, 43, 77–82. http://access.bl.uk/ark:/81055/vdc_100087066549.0x000044