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Specifically, these studies identified a G-to-A mutation at nucleotide positions 1896 or 1898, converting tryptophan (TGG) to a stop codon (TAG), leading to the absence of HBeAg[34, 35]

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[DOI] [PMC free article] [PubMed] [Google Scholar] 137.Ni Z., Anini Y., Fang X., Mills G., Brubaker P.L., Jin T