Article
Genetic origin of α0-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart's hydrops fetalis syndrome.
Journal of human genetics - 1 Aug 2017
Jomoui Wittaya, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Charoenwijitkul Patnaree, Maneesarn Jitpanu, Xu Xiangmin, Fucharoen Supan
Abstract excerpt
α0-thalassemia of SEA deletion (-SEA) is common among Southeast Asian and Chinese. Using haplotype and phylogenetic analyses, we examined the origin of this defect in Southeast Asian populations. Study was done on both normal and α0-thalassemia alleles in 3 ethnic groups including 96 Thai, 52 Laotian and 21 Cambodian. Five SNPs encompassing the (-SEA) including (rs3760053 T>G), (rs1211375 A>C), (rs3918352 A>G),...
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