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. 2018 Mar 13;6(1):35–42. doi: 10.1016/j.gendis.2018.03.003

Figure 1.

Figure 1

Identification of EGLN1 mutation in patients with cyanotic congenital heart disease. Results are presented with template strand which is opposite to the coding strand, so the remarked sign is changing C into G. (A). Sequencing results of EGLN1 c.380G>C mutation in 46 patients. (B) Sequencing results of wild-type DNA mutation in 80 patients.