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High SVR rates with eight and twelve weeks of pangenotypic glecaprevir/pibrentasvir: integrated efficacy and safety analysis of genotype 1–6 patients without cirrhosis

2017-01-01

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Literature Corpus work
d53bae3a-fa9f-5590-8c20-bf5d1a3b4bc3
DOI
10.1016/s0168-8278(17)31927-x
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High SVR rates with eight and twelve weeks of pangenotypic glecaprevir/pibrentasvir: integrated efficacy and safety analysis of genotype 1–6 patients without cirrhosisDOI 10.1016/s0168-8278(17)31927-x
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