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An update on the H blood group system

Paid access
|Feb 2020

References

  1. Scharberg EA, Olsen C, Bugert P. The H blood group system. Immunohematology 2016;32:112–8.
  2. Zanjani DS, Afzal Aghaee M, Badiei Z, et al. Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion. Vox Sang 2016;111:88–92.
  3. Michalewska B, Olsson ML, Naremska G, et al. FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon. Blood Transfus 2018;16:101–4.
  4. Hustinx H, Stettler J, Henny C, et al. Two cases of Caucasian Bombay and three cases of para-Bombay phenotype revealed five novel FUT1 alleles. Vox Sang 2018;113(Suppl 1):244.
  5. Lin F, Sun C, Wang H, Zhang X, Li J. Study of a case with homozygous 35C>T and 658C>T mutations of FUT1 gene leading to a para-Bombay phenotype. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2015;32:834–6.
  6. Wang L, Huang C, Wei Z, Tan J, Qin L, Tian L. Identification of a novel FUT1 allele with two mutations in a Chinese para-Bombay individual. Transfusion 2017;57:93–6.
  7. Lin J, Chen R, Zhu S, Qiu X, Huang Y, Wang X. Sequence analysis of α-(1,2)-fucosyltransferase gene in nine Chinese individuals with Para-Bombay phenotype. Gene 2018;685: 21–3.
DOI: https://doi.org/10.21307/immunohematology-2020-017 | Journal eISSN: 1930-3955 | Journal ISSN: 0894-203X
Language: English
Page range: 67 - 68
Published on: Feb 15, 2020
Published by: American National Red Cross
In partnership with: Paradigm Publishing Services
Publication frequency: 4 times per year

© 2020 E.A. Scharberg, C. Olsen, P. Bugert, published by American National Red Cross
This work is licensed under the Creative Commons License.