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Article

c.5del mutation on the ABO*B.01 allele responsible for Bx phenotype.

Transfusion - 1 Feb 2023

Li Yang, Wang Qiushi

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Identifiers

PMID: 36585797
DOI: 10.1111/trf.17231
PMCID: PMC10107131

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Research trail→

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c.5del mutation on the ABO*B.01 allele responsible for Bx phenotype.PMID 36585797Read ↗

Identification of a novel B allele with a c.586T>C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

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

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

Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.Semantic proximity Read ↗

c.125_126insT mutation in ABO*B.01 allele responsible for Bel 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 ↗

A novel B variant allele with c.586T>C (p.Cys196Arg) mutation identified at the ABO locus.Semantic proximity Read ↗

Identification of a novel B allele with a nucleotide deletion (c.103_106 delG) in the ABO gene associated with a B weak 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 ↗

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