Peter Young

A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies

G. Assmann, H. Wiebusch, H. Funke, 1997, Neurology.

Mutation analysis in Charcot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity

G. Kuhlenbäumer, H. Funke, O. Debus, 2001, Journal of Neurology.