Background CGG expansions in NOTCH2NLC and LRP12 were recently identified as a cause of Charcot-Marie-Tooth disease (CMT) in 1.2%–10.6% of genetically undiagnosed patients in China, Taiwan and Japan.

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Diffuse brain connectivity changes in Charcot-Marie-Tooth type 1a patients: a resting-state functional magnetic resonance imaging study.

Background and objectives Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy and often presents during childhood. Guidelines for the optimal management of common problems ...

Iconographie photographique de la Salpêtrière : service de M. Charcot by Regnard, Paul, 1850-1927; Bourneville, 1840-1909; Royal College of Physicians of Edinburgh ...