E. R. Swan

Neuropathy progression in Charcot-Marie-Tooth disease type 1A

M. Mcdermott, M. Mcdermott, D. Herrmann, 2008, Neurology.

CMT1X phenotypes represent loss of GJB1 gene function

S. Scherer, P. Ainsworth, M. Shy, 2007, Neurology.

CMT 1 X phenotypes represent loss of GJB 1 gene function

S. Scherer, P. Ainsworth, M. Shy, 2007 .

Women and men are equally disabled by Charcot–Marie–Tooth disease type 1A

M. Shy, D. Fuerst, E. R. Swan, 2007, Neurology.