Molecular characterization of hemoglobin C in Thailand

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Abstract

We describe hematologic and DNA characterization of 12 hemoglobin C heterozygotes and three compound heterozygotes for hemoglobin C and hemoglobin E found in Thailand. Amplification and DNA analysis of genomic DNA by the polymerase chain reaction procedure permitted the identification of the βc mutation at codon 6 of β-globin gene (β 6; GAG-AAG). β-Globin gene haplotype analysis demonstrated that all βc globin genes detected in these Thai individuals were associated with the haplotype (+ - - - - - +), indicating a non-African origin of this abnormal hemoglobin in Thailand. On routine hemoglobin typing, hemoglobin C is usually mistakenly identified as hemoglobin E because of theirs similar mobilities on cellulose acetate electrophoresis. The simple DNA assay for hemoglobin C based on an allele-specific polymerase chain reaction for accurate diagnosis of hemoglobin C was therefore developed. © 2001 Wiley-Liss, Inc.

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Sanchaisuriya, K., Fucharoen, G., Nattaya Sae-ung, N., Siriratmanawong, I., Surapot, S., & Fucharoen, S. (2001). Molecular characterization of hemoglobin C in Thailand. American Journal of Hematology, 67(3), 189–193. https://doi.org/10.1002/ajh.1105

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