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Abstract
In a sample of 6,156 sequences from 4,183 persons, the top 30 patterns of protease inhibitor, nucleoside reverse transcriptase (RT) inhibitor, and nonnucleoside RT inhibitor mutations accounted for 55, 46, and 66%, respectively, of sequences with drug resistance mutations. Characterization of the phenotypic and clinical significance of these common patterns may lead to improved treatment recommendations for a large proportion of patients for whom antiretroviral therapy is failing.
View details for DOI 10.1128/AAC.48.8.3122-3126.2004
View details for Web of Science ID 000222998300049
View details for PubMedID 15273130
View details for PubMedCentralID PMC478552