News

jmg.bmj1d
Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12–q13.3
2 Division of Neurology, Marqués de Valdecilla University Hospital, University of Cantabria, Santander, Spain 3 Division of Neurology, University Hospital Antwerp (UZA), Antwerp, Belgium ...
BMJ18d
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis
Background The international Inherited Neuropathy Consortium (INC) was created with the goal of obtaining much needed natural history data for patients with Charcot-Marie-Tooth (CMT) disease. We ...