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. 2015 Jan 1;60(4):323–327. doi: 10.1590/2359-3997000000108

Figure 1. Mutations in SLC26A4 in patients with CH. Figures (P1-P8) showed different sequences in identified eight affected individuals. P1, P2 showed the same SLC26A4 heterozygous mutation p.V233L. P3, P4 showed the same SLC26A4 heterozygous mutation p.P469S. P5, P6 showed heterozygous mutations p.M147I and p.V609G, respectively. P7, P8 showed the same SLC26A4 heterozygous mutation p.D661E.

Figure 1