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- W1553652025 abstract "Summary Introduction: Sudan has a multiethnic population with a high frequency of Hb S, but little is known about the β S haplotypes in this population. Methods: Blood samples from Sudanese Hb SS individuals were taken at two locations. Family history, age, ethnicity and clinical symptoms were recorded for each subject. Hb S was investigated using cellulose acetate electrophoresis (CAE) and cation exchange–high performance liquid chromatography. Dried blood samples from 93 individuals were used for β S haplotype identification based on restriction fragment length polymorphism analysis for seven restriction sites. Results: Haplotypes could be assigned unequivocally to 143 chromosomes. Four of the five typical β S ‐globin haplotypes were identified. The most frequent was the Cameroon (35.0%), followed by the Benin (29.4%), the Senegal (18.2%) and the Bantu (2.8%). The Indian‐Arab haplotype was not observed. Three atypical haplotypes were identified in 17 patients, occurring at a combined frequency of 14.6%. One of these, found at the high frequency of 11.8%, possibly represented a new Sudan haplotype. Conclusion: β S Haplotyes were demonstrated successfully from dried blood samples. A new haplotype is apparent in Sudan, in addition to the four African haplotypes." @default.
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- W1553652025 date "2012-01-20" @default.
- W1553652025 modified "2023-10-16" @default.
- W1553652025 title "Molecular analysis of the β-globin gene cluster haplotypes in a Sudanese population with sickle cell anaemia" @default.
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- W1553652025 doi "https://doi.org/10.1111/j.1751-553x.2011.01388.x" @default.
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