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. 2008 Sep 23;36(18):6004–6012. doi: 10.1093/nar/gkn595

Figure 6.

Figure 6.

Mechanisms to explain the sequence specificity of −2 deletion mutations. (a) Two possible misalignment-mediated pathways to explain the high frequency of the observed −2 deletion in the bypass of F flanked by T′s (5′-TFT-3′). (b) G misinsertion-mediated mechanism for all sequences.