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. 2019 Mar 12;10:259. doi: 10.3389/fphar.2019.00259

FIGURE 2.

FIGURE 2

Targeted sequencing-based identification of pathogenic variants. (A) Workflow for the analysis of targeted sequencing data. (B) The SNVs and InDels identified by targeted sequencing. (C) The number of missense and synonymous SNVs in coding regions.