Associated Papers
Identification and analysis of a novel A allele with a c.565A > G variant on the ABO*A1.02 allele leading to subtype A: A case report.
Lu W et al.
Medicine, 2025
Identification of a novel A allele with a c.421T>C variant on the ABO*A1.02 allele in a Chinese individual.
Ou G et al.
Transfusion, 2024
Characterization of a novel AEL allele harboring a c.28 + 5G>A mutation on the ABO*A2.01 background: a study utilizing PacBio third-generation sequencing and functional assays.
Shao LN et al.
Frontiers in Immunology, 2024
A new missense variant c.278C > G on the ABO*B.01 allele associated with a Bel phenotype.
He Y et al.
Transfusion, 2023
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants.
Gueuning M et al.
Blood Advances, 2023
RBCeq: A robust and scalable algorithm for accurate genetic blood typing.
Jadhao S et al.
Ebiomedicine, 2022
Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.
Liang S et al.
Transfusion, 2021
Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.
Möller M et al.
Vox Sanguinis, 2018
Molecular genetic analysis and structure model of a rare B(A)02 subgroup of the ABO blood group system.
Chen Q et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2014
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