An autosome-wide search using longitudinal data for loci linked to type 2 diabetes progression |
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Authors: | Jun Gyungah Song Yeunjoo Stein Catherine M Iyengar Sudha K |
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Institution: | 1. From the Department of Transfusion Medicine, University Hospital, Ulm, Germany 2. Institute for Clinical Transfusion Medicine and Immunogenetics, Ulm, Germany 5. Blood Service of the German Red Cross N.S.T.O.B., Springe, Germany 3. Department of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, USA 4. Centre National de Transfusion Sanguine, Bamako, Mali
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Abstract: | Background Aberrant and non-functional RHD alleles are much more frequent in Africans than in Europeans. The DAU cluster of RHD alleles exemplifies that the alleles frequent in Africans have evaded recognition until recently. A comprehensive survey of RHD alleles in any African population was lacking. Results We surveyed the molecular structure and frequency of RHD alleles in Mali (West Africa) by evaluating 116 haplotypes. Only 69% could be attributed to standard RHD (55%) or the RHD deletion (14%). The aberrant RHD allele DAU-0 was predicted for 19%, RHDΨ for 7% and Ccde s for 4% of all haplotypes. DAU-3 and the new RHD allele RHD(L207F), dubbed DMA, were found in one haplotype each. A PCR-RFLP for the detection of the hybrid Rhesus box diagnostic for the RHD deletion in Europeans was false positive in 9 individuals, including all carriers of RHDΨ . Including two silent mutations and the RHD deletion, a total of 9 alleles could be differentiated. Conclusion Besides standard RHD and the RHD deletion, DAU-0, RHDΨ and Ccde s are major alleles in Mali. Our survey proved that the most frequent alleles of West Africans have been recognized allowing to devise reliable genotyping and phenotyping strategies. |
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