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D L Sherman

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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.

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.

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Search research articles

Showing results (31-40 of 32) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 32 results.

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.

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.

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