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. Author manuscript; available in PMC: 2020 Apr 15.
Published in final edited form as: J Neurol Sci. 2020 Jan 14;411:116687. doi: 10.1016/j.jns.2020.116687

Figure 2. Uncommon (rare) “singleton” SNV found in cases (red) or controls (blue) across 49 canonical CMT-associated genes.

Figure 2.

Genes are ordered according to the excess of mutations found in cases (top) to excess in controls (bottom).