Associated Papers
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
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
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeI-
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
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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