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Article

ABO gene mutation c.815_816insG in an African individual forms a novel Ael allele.

Transfusion - 1 Jul 2021

Lei Hang, Lu Qiong, Xiang Dong, Wang Xuefeng, Cai Xiaohong

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Share to ABO Blood-Group System
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 33899249
DOI: 10.1111/trf.16419

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Related research

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Research trail→

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ABO gene mutation c.815_816insG in an African individual forms a novel Ael allele.PMID 33899249Read ↗

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

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

A novel ABO insertion c.797insT giving rise to an Ael phenotype.Semantic proximity Read ↗

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

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

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Identification of a novel ABO*A1.02 allele with variant c.671T>C.Semantic proximity Read ↗

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