Associated Papers
Molecularly confirmed para-Bombay (Ah) secretor phenotype with FUT1 c.328G>A and FUT2 c.357C>T mutations: first case report from India.
Arivazhagan T et al.
Blood Transfusion = Trasfusione Del Sangue, 2025
[Identification of a novel FUT1 allele in a Chinese individual featuring para-Bombay phenotype].
Li Q et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2022
Two novel alleles on Fucosyltransferase 2 from northern Thai para-Bombay family and computational prediction on mutation effect.
Anukul N et al.
Transfusion, 2021
[Serological Identification and FUT1 Gene Mutation Analysis of 8 Individuals with Para-Bombay Phenotypes in Guangxi].
Liu JL et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2021
A Para-Bombay Blood Group Case Associated with a Novel FUT1 Mutation c.361G>A.
Lei H et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2021
The First Case of Para-Bombay Blood Type Encountered in a Korean Tertiary Hospital.
Kim MS et al.
Journal of Korean Medical Science, 2019
A Very Rare Case with Particular H-deficient Phenotypes.
Song M et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion, 2018
FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon.
Michalewska B et al.
Blood Transfusion = Trasfusione Del Sangue, 2018
Genomic analysis of para-Bombay individuals in south-eastern China: the possibility of linkage and disequilibrium between FUT1 and FUT2.
Zhang A et al.
Blood Transfusion = Trasfusione Del Sangue, 2015
Two Novel α 1,2-Fucosyltransferase Alleles in an H-Deficient Phenotype Individual.
He Z et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2014
The summary of FUT1 and FUT2 genotyping analysis in Chinese para-Bombay individuals including additional nine probands from Guangzhou in China.
Luo G et al.
Transfusion, 2013
H blood-group deficiency has a high frequency in Lahu Chinese.
Cai XH et al.
Transfusion Medicine (oxford, England), 2011
Novel mutations, including a novel G659A missense mutation, of the FUT1 gene are responsible for the para-Bombay phenotype.
Sun CF et al.
Annals of Clinical and Laboratory Science, 2000
Two missense mutations of H type alpha(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype.
Wang B et al.
Vox Sanguinis, 1997