Novel missense mutation c.797T>C (p.Met266Thr) gives rise to the rare B(A) phenotype in a Chinese family.
Lin-Nan ShaoYi-Cheng YangYue-Xin XiaChun-Xiang LiShi-Hang ZhouXiao-Hua LiangPublished in: Vox sanguinis (2024)
The probands had the same novel B(A) allele with a c.797T>C (p.Met266Thr) mutation on the ABO*B.01 backbone.
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