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. 2017 Jul 3;12(7):e0180237. doi: 10.1371/journal.pone.0180237

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© 2017 Jang et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 2 — DNA amplification with Q-fever-IS1111a primers for the detection of Coxiella burnetii. Gel electrophoresis of 202 bp products by using end-point PCR. M: 50bp DNA size marker; 1–11: DNAs from the case patients with Q fever hepatitis and N: negative control (left). M: 50bp DNA size marker; PC: C. burnetii DNA control (case number 1 of case patient group); 1–10: DNAs from the control patients and N: negative control (right).