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Human Molecular Genetics|February 7, 2001
A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth diseaseA Guilbot, A Williams, N Ravisé, et al.Journal of Neuroscience Research|October 1, 1992
Developmental expression of major myelin protein genes in the CNS of X-linked hypomyelinating mutant rumpshakerL S Mitchell, S C Gillespie, F McAllister, et al.Neuron|June 6, 2000
Peripheral demyelination and neuropathic pain behavior in periaxin-deficient miceC S Gillespie, D L Sherman, S M Fleetwood-Walker, et al.Pageof 7