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[The result demonstrated that multiple genetic modifying factors including T allele of (G)?-XmnI polymorphism (rs7482144), G allele of HBS1L-MYB (rs489441), C allele of HBS1L-MYB (rs9399137) and C allele of BCL11A (rs4671393) are associated with increased Hb F and in combination could explain approximately 80% of the variation of Hb F in Hb EE disease in Thai population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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