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Mutations in the netrin 1 gene cause congenital mirror movements

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Figure

Figure 1. Pedigrees of the CMM families and distribution of the mutations in NTN1. (A) Family 1 (from France) with a C601R mutation (the unusual family tree is a result of individual 1.1, who had children with 4 different women), (B) family 2 (from the Uni
Table 1. Summary of the NTN1 mutations identified in patients with CMM
Figure 2. Position and conserva-tion of the mutated amino acids.
Figure 3. CST analysis using tractography. (A) Illustration of crossed (blue) and uncrossed (red) CSTs
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