Rare P k phenotype caused by a novel frameshift mutation in B3GALNT1
Author:
Affiliation:
1. Department of Transfusion Research Jiangsu Province Blood Center Nanjing China
2. Department of Transfusion Medicine The First People's Hospital of Lianyungang Lianyungang China
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/tme.12895
Reference7 articles.
1. Molecular Basis of the Globoside-deficient Pk Blood Group Phenotype
2. Pedigree investigation and genetic analysis of a case with P blood group;Liu YC;Zhonghua Yi Xue Yi Chuan Xue Za Zhi,2013
3. Molecular basis for the p and Pkphenotypes in three Chinese individuals
4. MutationTaster evaluates disease-causing potential of sequence alterations
5. Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus
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