First observation of a mutation (L26F) in a weak D phenotype encoded by 76 C>T, ethnic origin: Austria. undefined
收藏NIAID Data Ecosystem2026-03-14 收录
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Sanger sequencing of RHD exons 1 to 10 and boundaries elucidated a novel C>T alteration at position 76 causing for a L26F amino acid alteration. According to the transmembraneous position of the alteration and an RhD antigen density of approximately 4.800 epitopes/cell, this allele enlarges the number of RHD weak D alterations.
创建时间：
2022-10-03
