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. 2016 Oct 4;242(3):267–274. doi: 10.1177/1535370216668052

Figure 5.

Figure 5

Relative transcriptional levels of miR-146a in CD34+-derived erythroid cells, as evaluated by quantitative reverse-transcription PCR (qRT-PCR). Taqman qRT-PCR was used to evaluate the levels of miR-146a. Controls = CTRL (n = 3); subjects heterozygous for HPFH-2 = HPFH-2 (n = 2); patients heterozygous for Sicilian δβ-thalassemia = DB-Thal (n = 2)