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c.586T>C mutation on the ABO*A1.02 allele responsible for Ael phenotype.

Transfusion - 1 Jun 2022

Shen Yuqing, Yang Xiaojun, Lu Chunjing, Chen Fawen, Ye Xianren, Su Naizhu

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PMID: 35470871
DOI: 10.1111/trf.16890

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

c.586T>C mutation on the ABO*A1.02 allele responsible for Ael phenotype.PMID 35470871Read ↗

A novel c.28 + 1G > T mutation in the ABO*A1.02 allele that results in Ael phenotype.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.36-39delA 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.423 C > A mutation on the ABO*A1.02 allele.Semantic proximity Read ↗

ABO gene mutation c.815_816insG in an African individual forms a novel Ael 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 ABO*A1.02 allele with variant c.671T>C.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 c.102C > A variation 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 ↗

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

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