Associated Papers
The protean presentations of XK disease (McLeod syndrome): a case series with new observations and updates on previously reported families.
Walker RH et al.
Frontiers in Neuroscience, 2024
A structure-based in silico analysis of the Kell blood group system.
Mayr G et al.
Frontiers in Immunology, 2024
Three new XK alleles; two associated with a McLeod RBC phenotype.
Floch A et al.
Transfusion, 2021
KEL*02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,-2 phenotypes.
Wester ES et al.
Vox Sanguinis, 2010
A KEL gene encoding serine at position 193 of the Kell glycoprotein results in expression of KEL1 antigen.
Poole J et al.
Transfusion, 2006
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