Peter J. Brophy

A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease.

A. Mégarbané, A. Brice, D. Sherman, 2001, Human molecular genetics.

Periaxin expression in myelinating Schwann cells: modulation by axon-glial interactions and polarized localization during development.

D. Sherman, S. Scherer, P. Bannerman, 1995, Development.

Disruption of neurofascin localization reveals early changes preceding demyelination and remyelination in multiple sclerosis.

P. Brophy, R. Reynolds, A. Palser, 2006, Brain : a journal of neurology.

Charcot–Marie–Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene

D. Sherman, P. Brophy, A. Kochański, 2006, Neurology.

Integrin-mediated axoglial interactions initiate myelination in the central nervous system

D. Sherman, C. Nunes-Fonseca, J. Câmara, 2009 .