Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransferase gene responsible for the p phenotype
Author:
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1537-2995.2002.00014.x/fullpdf
Reference15 articles.
1. 1. G Daniels . Human blood groups . Oxford: Blackwell, 1995 :227 -56 .
2. Molecular Cloning of Globotriaosylceramide/CD77 Synthase, a Glycosyltransferase That Initiates the Synthesis of Globo Series Glycosphingolipids
3. Cloning and Expression of the Histo-blood Group PkUDP-galactose:Galβ1–4Glcβ1-Cer α1,4-Galactosyltransferase
4. Molecular Basis for the p Phenotype
5. Simple PCR detection of haptoglobin gene deletion in anhaptoglobinemic patients with antihaptoglobin antibody that causes anaphylactic transfusion reactions
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1. Two Thai Burmese descendants with A4GALT*01N.21, p phenotype, and anti-PP1Pk;Immunohematology;2020
2. Anti-PP1Pk(Tja) Antibody in a Korean Female Patient with p Phenotype Confirmed by Genotyping;Laboratory Medicine Online;2020
3. The mutation and one-base insertion of the α(1,4)galactosyltransferase gene responsible for the p phenotype;Transfusion Clinique et Biologique;2019-11
4. First Case in Korea of a Patient With Anti-PP1Pk Antibodies: Successful Blood Management via Acute Normovolemic Hemodilution;Annals of Laboratory Medicine;2019-11-01
5. Human genetic disorders of sphingolipid biosynthesis;Journal of Inherited Metabolic Disease;2014-08-21
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