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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.

Transfusion - 1 Oct 2023

Li Ying, Zhu Yongliang, Xu Jinming, Zhou Xiaoyu

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Identifiers

PMID: 37665199
DOI: 10.1111/trf.17517

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

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.PMID 37665199Read ↗

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

Identification of a novel A allele with a c.102C > A variation on the ABO*A1.02 allele.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 A allele with a c.36-39delA on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene.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 ↗

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

Identification of a novel A allele with c.478C>T missense mutation on the ABO*A1.02 background.Semantic proximity Read ↗

Identification of a novel A allele with a nucleotide deletion c.198delG in the ABO gene associated with Ael phenotype.Semantic proximity Read ↗

Identification of a novel a variant at the ABO locus in Chinese Han individuals with a A2 phenotype.Semantic proximity Read ↗

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