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…s 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 Chin…

… variants in SLC12A6 have recently been shown to cause dominant Charcot-Marie-Tooth disease (CMT). We aim to characterise the phenotype of patients with pr…

…rsus HC (all p<0.01). Periaxin was elevated in two out of eight CMT2A patients, two out of eight CMTX patients, and below detection l…

… studies in inherited neuropathies. The expanding phenotypes in dHMN and CMT, with previous work in sigma nonopiod intracellular rec…

…Charcot-Marie-Tooth disease (CMT) is a group of inherited disorders that cause progressive …

…easure anterior chamber flare (ACF). Central macular thickness (CMT) was assessed using optical coherence tomography. To quantify p…

…Charcot–Marie–Tooth (CMT) disease is a progressive hereditary neuropathy that compl…