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The paper published by the ANRS 12235 Study Group ([1][1]) showed that monitoring of “real-life” HIV-1 RNA viral load (VL) and drug resistance mutations (DRMs) in dried blood spot (DBS) specimens collected from patients in Africa and Asia was possible, but with some limitations, particularly for

journal of clinical microbiology

Use of Reverse Transcription-PCR-Based Assays for Quantification of HIV-1 in Dried Blood Spots Requires Specific HIV-1 RNA Isolation for Monitoring of Antiretroviral Treatment Efficiency