First observation of a mutation (P221A) in a weak D phenotype encoded by 661 C>G, ethnic origin: Austria. RHD sequencing
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https://www.ncbi.nlm.nih.gov/bioproject/PRJEB55786
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资源简介：
Sanger sequencing of RHD exons 1 to 10 and boundaries elucidated a novel C>G alteration at position 661causing for a P221A amino acid alteration. According to the transmembraneous position of the alteration and an RhD antigen density of approximately 2.000 epitopes/cell, this allele enlarges the number of RHD weak D alterations.
创建时间：
2022-09-20
