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From: Genetic approaches and pathogenic pathways in the clinical management of Charcot-Marie-Tooth disease
Figure 1. Schematic summary of genes causing CMT hereditary neuropathy. Gene products are assigned either to the neuron body and axon or to the myelinating Schwann cell (cross-sectional view in box). Proteins are classified according to their main functions or pathways and their proposed pathomechanisms in CMT. The most commonly involved genes are indicated in bold. More information about each gene and/or protein is available in Table 2 and Supplementary Table 1. ER: Endoplasmic reticulum. Illustration created with BioRender (Available from: https://biorender.com/).
