RhD alloimmunization by DEL variant missed in donor testing.

Hana Safic StanicVesna DogicJasna Bingulac-PopovicZrinka Kruhonja GalicMiljana Stojic VidovicKresimir PuljicIrena Jukic

Published in: Transfusion (2022)

Currently used methods in RHD genotyping are insufficient to identify many variant alleles, especially intronic variations. We suggest additional gene investigation including yet unexplored regions of regulation and intron regions to justify our serological finding.

Keyphrases

genome wide
copy number
high throughput
sickle cell disease
dna methylation
genome wide analysis