Associated Papers
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
A new h allele detected in Europe has a missense mutationin alpha(1,2)-fucosyltransferase motif II.
Wagner T et al.
Transfusion, 2001
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
Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South Africa.
Pang H et al.
Human Genetics, 1998
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
Two missense mutations of H type alpha(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype.
Wang B et al.
Vox Sanguinis, 1997
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