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 missense variant (c.567G>A, p. Met189Ile) in ABO*B.01 allele.
Wang H et al.
Transfusion, 2025
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