Abstract
IN an earlier communication1, we reported two sisters having the Kell phenotype K–,k–,Kp(a–b–). The parents were second cousins, and it was assumed that the sisters were homozygous for a Kell gene the product of which does not react with any of the known Kell antisera. Allen et al. 2 later gave this gene the abbreviation K0. Alternatively, there may be a deletion or suppression. We have sought for other examples of this phenotype by using the serum of the propositus of the above family by the capillary–papain method3; by this method the serum reacts with all K+ or k+ bloods. The 3,122nd blood so tested did not react, indicating that it was of the phenotype we sought. This was confirmed by testing with anti-K, anti-k, anti-Kpa and anti-kpb; it reacted with none of these.
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References
Chown, B., and Lewis, Marion, and Kaita, Hiroko, Nature, 180, 711 (1957).
Allen, jun., Fred H., Lewis, Sheila J., and Fudenberg, H., Vox Sang., 3, 1 (1958).
Lewis, Marion, Kaito, Hiroko, and Chown, B., J. Lab. Clin. Med., 52, 163 (1958).
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KAITA, H., LEWIS, M., CHOWN, B. et al. A Further Example of the Kell Blood Group Phenotype K–,k–,Kp(a–b–). Nature 183, 1586 (1959). https://doi.org/10.1038/1831586b0
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DOI: https://doi.org/10.1038/1831586b0
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