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Article

A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with Bw phenotype.

Transfusion - 1 Oct 2022

Hult Annika K, Hellberg Åsa, Storry Jill R, Písacka Martin, Olsson Martin L

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

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PMID: 36125051
DOI: 10.1111/trf.17109
PMCID: PMC9826363

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with Bw phenotype.PMID 36125051Read ↗

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ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype.Semantic proximity Read ↗

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