C35T mutation could slightly decrease the activity of human α-(1,2)-fucosyltransferase
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Hematology
Reference16 articles.
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2. Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals;Kelly;Proc Natl Acad Sci U S A,1994
3. Sequence and expression of a candidate for the human Secretor blood group alpha(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype;Kelly;J Biol Chem,1995
4. Molecular cloning of a human genomic region containing the H blood group alpha(1,2)fucosyltransferase gene and two H locus-related DNA restriction fragments. Isolation of a candidate for the human Secretor blood group locus;Rouquier;J Biol Chem,1995
5. Molecular genetic basis of the histo-blood group ABO system;Yamamoto;Nature,1990
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1. Identification of two novel FUT1 mutations in people with Bombay phenotype from Iran;Transfusion and Apheresis Science;2023-06
2. Two novel alleles on Fucosyltransferase 2 from northern Thai para‐Bombay family and computational prediction on mutation effect;Transfusion;2021-09-06
3. Interaction of genetic markers associated with serum alkaline phosphatase levels in the Japanese population;Human Genome Variation;2015-07-02
4. Two Novel a1,2-Fucosyltransferase Alleles in an H-Deficient Phenotype Individual;Transfusion Medicine and Hemotherapy;2014
5. Erratum to “C35 T mutation could slightly decrease the activity of human α-(1, 2)-fucosyltransferase”;Transfusion Clinique et Biologique;2012-04
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