Molecular basis for para-Bombay phenotypes in Chinese persons, including a novel nonfunctionalFUT1allele
Author:
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1537-2995.2005.04305.x/fullpdf
Reference23 articles.
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2. Molecular cloning, sequence, and expression of a human GDP-L-fucose: beta-D-galactoside 2-alpha-L-fucosyltransferase cDNA that can form the H blood group antigen;Larsen;Proc Natl Acad Sci U S A,1990
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 basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals;Kelly;Proc Natl Acad Sci U S A,1994
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3. Two novel alleles on Fucosyltransferase 2 from northern Thai para‐Bombay family and computational prediction on mutation effect;Transfusion;2021-09-06
4. Landsteinerʼs legacy: The continuing challenge to make transfusions safe;Transfusion;2020-12
5. Two novel FUT1 alleles that cause para‐Bombay phenotype in a Chinese individual;Transfusion;2020-11-11
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