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Identification of a novel c.259G > T mutation in the ABO*B.01 allele giving rise to a B3 phenotype.

Transfusion - 1 Jul 2022

Liu Hongbo, Liu Fengxia, Chen Wei, Zhou Shiqiao, Xiao Xiaohong, Chen Wei, Dai Xiaohui, Li Xiong, Liu Hongmei

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PMID: 35713154
DOI: 10.1111/trf.16948

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a novel c.259G > T mutation in the ABO*B.01 allele giving rise to a B3 phenotype.PMID 35713154Read ↗

Identification of a novel B allele with a c.256G>A mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel B allele with a c.586T>C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel B allele with a c.917 T > C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel A allele with a c.423 C > A mutation on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel A allele with a c.731T>C mutation on the ABO*A1.02 allele.Semantic proximity Read ↗

ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype.Semantic proximity Read ↗

Identification of a novel A allele with a nucleotide insert (c.99-1_100 T) in the ABO gene associated with a A3 phenotype individual.Semantic proximity Read ↗

A novel B variant allele with c.586T>C (p.Cys196Arg) mutation identified at the ABO locus.Semantic proximity Read ↗

Identification of a novel A allele with a c.977A>C variation on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel c.77T>G mutation on the ABO*B.01 allele associated with a B subtype.Semantic proximity Read ↗

Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel B allele with a nucleotide deletion (c.103_106 delG) in the ABO gene associated with a B weak phenotype.Semantic proximity Read ↗

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