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Article

A novel KEL null allele with c.223+1g>t leads to the absence of the Kpb antigen in a First Nation donor.

Transfusion - 1 Sept 2021

Leiva-Torres Gabriel André, Lavoie Josée, Ethier Carole, Constanzo-Yanez Jessica, Baillargeon Nadia

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PMID: 34310722
DOI: 10.1111/trf.16604

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Related research

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Research trail→

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A novel KEL null allele with c.223+1g>t leads to the absence of the Kpb antigen in a First Nation donor.PMID 34310722Read ↗

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Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K0 (Kellnull ) phenotypes.Semantic proximity Read ↗

Two novel KEL alleles encoding K0 phenotypes in Brazilians.Semantic proximity Read ↗

Novel KEL*02N allele in Saudi Arabia encoding a Kell null (K0 ) phenotype.Semantic proximity Read ↗

Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American.Semantic proximity Read ↗

Molecular basis of the Kell-null phenotype: a mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigens.Semantic proximity Read ↗

Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 alleles.Semantic proximity Read ↗

Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.Semantic proximity Read ↗

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Five novel silenced KEL*02 alleles.Semantic proximity Read ↗

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