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Article

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

Transfusion - 1 Jan 2023

Ma Wenhui, Zhao Wei, Feng Zhihui, Bu Xiangmao

Abstract excerpt

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Topics

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Share to ABO Blood-Group System
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Share to East Asian People
Share to ABO gene

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 36504115
DOI: 10.1111/trf.17214

Genes

ABO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a novel a variant at the ABO locus in Chinese Han individuals with a A2 phenotype.PMID 36504115Read ↗

Identification of novel variant A alleles within the ABO gene.Semantic proximity Read ↗

Identification of a novel A allele with a c.421T>C variant on the ABO*A1.02 allele in a Chinese individual.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 novel variant B alleles within the ABO gene.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.102C > A variation on the ABO*A1.02 allele.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 ↗

Identification of a novel A allele with initiator codon variant (c.2T > A) in the ABO gene associated with weak A phenotype.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 nucleotide deletion c.198delG in the ABO gene associated with Ael phenotype.Semantic proximity Read ↗

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 B allele with missense mutation (c.98G > C) in the ABO gene.Semantic proximity Read ↗

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