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Article

Bw phenotype associated with novel start codon variant of ABO gene.

Transfusion - 1 Jun 2023

Wu Wen, Huang Xiangyan

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Identifiers

PMID: 37083236
DOI: 10.1111/trf.17361

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Bw phenotype associated with novel start codon variant of ABO gene.PMID 37083236Read ↗

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

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

Identification of a novel A allele with initiator codon variant (c.2T > A) in the ABO gene associated with weak A phenotype.Semantic proximity Read ↗

Identification of novel variant B alleles within the ABO gene.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 ↗

c.125_126insT mutation in ABO*B.01 allele responsible for Bel phenotype.Semantic proximity Read ↗

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

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Identification of a novel missense mutation (563G>a) in the ABO gene associated with a Bel phenotype.Semantic proximity Read ↗

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A novel variant B allele at the ABO gene locus characterized by a duplication-based insertion of 27 nucleotides identified in an Iraqi male with a weak B subgroup phenotype.Semantic proximity Read ↗

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