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BACKGROUND
Molecular tests designed to detect the presence of active RHD gene among D– donors have been successfully applied in people of European ancestry, but not in admixed populations with a considerable frequency of RHD*Ψ. Our goal was to evaluate the performance of a molecular screening tool for identifying active RHD alleles among Brazilian blood donors classified as D– C+ and/or E+.
STUDY...
The complexity of Rh genetic variation among sickle cell disease (SCD) patients is high. Conventional molecular assays cannot identify all genetic variants already described for the RH locus as well as foresee novel alleles. Sequencing RHD and RHCE is indicated to broaden the search for Rh genetic variants.To standardize the Next Generation Sequencing (NGS) strategy to assertively identify Rh genetic...
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