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[A significant difference in the incidence of mEH slow allele variant was observed between case control group (15/38, 39 %) and esophageal dysplasia group (22/32, 69 %) or ESCC group (39/62, 63 %) (P<0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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