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pylori DNA was evaluated by nested PCR utilizing primers designed to amplify H. pylori-specific segments throughout the bacterial 16S rDNA. The exterior primers utilized in first-spherical PCR have been EHC-U and EHC-L, while in the second round of DNA amplification, it was used primers ET-5U and ET-5L producing a 230-bp fragment throughout the amplicon of the primary-round PCR. The prevalence of this bacterium was related to socioeconomic conditions, regardless of gender and ethnicities, being extra frequent in low earnings folks, and subjects

 

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