Novel RHD allele with c.487‐2A>G (IVS3‐2A>G) variant causing RhD negative phenotype
Author:
Affiliation:
1. Institute of Transfusion Medicine Qingdao Blood Center Qingdao China
2. Department of Blood Transfusion Qingdao Eighth People's Hospital Qingdao China
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.17979
Reference5 articles.
1. Molecular basis of theRHDgene in blood donors with DEL phenotypes in Shanghai
2. RHD gene deletion occurred in the Rhesus box
3. A newRHDvariant allele in Exon 2 identified in a Chinese individual
4. Multiple isoforms excluding normal RhD mRNA detected in Rh blood group Del phenotype with RHD 1227A allele
5. Missense RHD single nucleotide variants induce weakened D antigen expression by altering splicing and/or protein expression
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