Associated Papers
C35T mutation could slightly decrease the activity of human α-(1,2)-fucosyltransferase.
Tao S et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2012
A novel FUT1 allele was identified in a Chinese individual with para-Bombay phenotype.
Xu X et al.
Transfusion Medicine (oxford, England), 2011
[Para-Bombay phenotype caused by combined heterozygote of two bases deletion on fut1 alleles].
Ma KR et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2011
Two prevalent h alleles in para-Bombay haplotypes among 250,000 Taiwanese.
Chen DP et al.
Annals of Clinical and Laboratory Science, 2004
The polymorphisms of fucosyltransferases.
Koda Y et al.
Legal Medicine (tokyo, Japan), 2001
Point mutations and deletion responsible for the Bombay H null and the Reunion H weak blood groups.
Fernandez-Mateos P et al.
Vox Sanguinis, 1998
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