Two novel FUT1 alleles that cause para‐Bombay phenotype in a Chinese individual
Author:
Affiliation:
1. Key Laboratory of Blood Safety Research of Liaoning Shenyang China
2. Liaoning Blood Center Shenyang China
3. Harbin Blood Center Harbin China
4. Department of Pharmacology School of Pharmacy, China Medical University Shenyang China
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.16183
Reference5 articles.
1. Molecular genetic basis of the histo-blood group ABO system
2. Sequence and Expression of a Candidate for the Human Secretor Blood Group α(1,2)Fucosyltransferase Gene (FUT2)
3. Wide Variety of Point Mutations in the H Gene of Bombay and Para-Bombay Individuals That Inactivate H Enzyme
4. Molecular basis for para-Bombay phenotypes in Chinese persons, including a novel nonfunctionalFUT1allele
5. Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Identification of two novel FUT1 mutations in people with Bombay phenotype from Iran;Transfusion and Apheresis Science;2023-06
2. Molecular Genetic Analysis of Para-Bombay Phenotype in Chinese: Identification of a Novel FUT1 Allele;Clinical Laboratory;2023
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