Associated Papers
Identification of a novel null allele A4GALT*02: c.457_463dup in one Chinese pedigree with the rare p phenotype and anti-PP1Pk.
Jin Y et al.
Transfusion, 2026
A case report of a rare p phenotype individual and a review of molecular biological analysis of p phenotype in the Chinese population.
Wei X et al.
Transfusion Medicine (oxford, England), 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
[Serological characteristics and molecular mechanism of an individual with p phenotype].
Tu J et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2023
Naturally occurring anti-PP1PK in a Chinese individual with p phenotype: A case based on compound heterozygosity including one novel allele.
Liang S et al.
Transfusion, 2022
[Pedigree investigation and genetic analysis of a case with p blood group].
Liu YC et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2013
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