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. 2017 Mar 28;88(13):1226–1234. doi: 10.1212/WNL.0000000000003772

Figure 2. Identified genes in our hereditary motor neuropathy (HMN) patient cohort.

Figure 2

(A) Spectrum and distribution of mutated genes detected in our cohort within the 3 phenotypic groups. (B) Overlapping clinical phenotypes related to the identified genes and key additional clinical features associated. *Upper motor neuron involvement. ALS = amyotrophic lateral sclerosis.