Associated Papers
Unveiling Novel and Rare Variants in the α-1,4-Galactosyltransferase Gene Leading to Rare p Phenotype in Indian Patients.
Kshirsagar P et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2025
Novel A4GALT Variants Cause Rare p Phenotype and Recurrent Pregnancy Loss in a Chinese Individual.
Li G et al.
American Journal of Medical Genetics. Part A, 2025
P-Null Phenotype Due to a Rare Frame-Shift Mutation and with Allo-Anti-PP1Pk Causing a Severe Hemolytic Transfusion Reaction: A Case Report with Clinical Management.
Kanani AN et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2021
P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.
Westman JS et al.
Transfusion, 2013
Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection.
Hellberg A et al.
British Journal of Haematology, 2004
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