Repeated clear benefits of immunotherapy in a patient with Charcot-Marie-Tooth disease carrying a rare point mutation in PMP22.

Moreover, peripheral T-cell responses to various myelin epitopes in a case of the coexistence of optic neuritis and CMT with duplication of the PMP22 gene were reported to show highly significant proliferation against the CNS myelin protein, proteolipid protein (PLP), which shares partial homology with PMP22 [ 5 ].

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