Rhnull syndrome: identification of a novel mutation in RHce.Katie Rosa, Megan E Reid, +8 authors Lilian CastilhoTransfusion2005BACKGROUND The deficiency of Rh proteins on red blood cells (RBCs) from individuals of the Rh(null) amorph type are the result of homozygosity for a silent RHCE in cis with a deleted RHD. A novel… (More)