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Blood ; 100(1): 306-11, 2002 Jul 01.
Article in English | MEDLINE | ID: mdl-12070041

ABSTRACT

Variant D occurs frequently in Africans. However, considerably less RHD alleles have been described in this population compared with Europeans. We characterized 5 new RHD alleles, dubbed DAU-0 to DAU-4, that shared a T379M substitution and occurred in a cDe haplotype. DAU-1 to DAU-4 were detected in Africans with partial D phenotypes. They harbored one and 2 additional missense mutations, respectively, dispersed throughout the RhD protein. An anti-D immunization was found in DAU-3. DAU-0 carrying T379M only was detected by screening European blood donors and expressed a normal D phenotype. Within the phylogeny of the RHD alleles, DAU formed an independent allele cluster, separate from the DIVa, weak D type 4, and Eurasian D clusters. The characterization of the RH phylogeny provided a framework for future studies on RH alleles. The identification of the DAU alleles increased the number of known partial D alleles in Africans considerably. DAU alleles may be a major cause of antigen D variability and anti-D immunization in patients of African descent.


Subject(s)
Alleles , Rh-Hr Blood-Group System/genetics , Africa/epidemiology , Amino Acid Substitution/immunology , Black People/genetics , Epitopes/genetics , Genetic Variation/genetics , Genetic Variation/immunology , Humans , Multigene Family , Phenotype , Phylogeny , Polymorphism, Single Nucleotide , Rh Isoimmunization/genetics , Rh-Hr Blood-Group System/immunology
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