The mutation and one-base insertion of the α(1,4)galactosyltransferase gene responsible for the p phenotype
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Hematology
Reference11 articles.
1. International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Berlin report;Storry;Vox Sang,2011
2. Human Gb3/CD77 synthase reveals specificity toward two or four different acceptors depending on amino acid at position 211, creating P(k), P1 and NOR blood group antigens;Kaczmarek;Biochem Biophys Res Commun,2016
3. Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles;Westman;Transfusion,2014
4. P1PK, GLOB, and FORS blood group systems and GLOB collection: biochemical and clinical aspects. Do we understand it all yet?;Kaczmarek;Transfus Med Rev,2014
5. Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotype;Hellberg;Transfusion,2008
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