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

Transfusion - 1 May 2024

Hao Xiao, Diao Xueqin, Cui Congcong, Lv Yihua, Liu Yueqin, Bi Huiwen

Abstract excerpt

No abstract is available from the source.

Topics

Humans
ABO Blood-Group System
Alleles
Mutation
Female
Male
Point Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 38650375
DOI: 10.1111/trf.17832

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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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.77T>G mutation on the ABO*B.01 allele associated with a B subtype.PMID 38650375Read ↗

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 B allele with a c.256G>A mutation on the ABO*B.01 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 ↗

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 c.423 C > A mutation 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 ABO*A1.02 allele with variant c.671T>C.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 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 c.478C>T missense mutation on the ABO*A1.02 background.Semantic proximity Read ↗

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