P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.

Julia Westman, Åsa Hellberg, Thierry Peyrard, Hein Hustinx, Britt Thuresson, Martin L Olsson

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskriftPeer review

Sammanfattning

The rare but clinically important null phenotypes of the P1PK and GLOB blood group systems are due to alterations in A4GALT and B3GALNT1, respectively. A recently identified single-nucleotide polymorphism in Exon 2a of A4GALT predicts the common P1 and P2 phenotypes but rare variants have not been tested.
Originalspråkengelska
Sidor (från-till)2928-2939
TidskriftTransfusion
Volym53
Nummer11
DOI
StatusPublished - 2013

Ämnesklassifikation (UKÄ)

  • Hematologi

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