Researchers are investigating whether treatments for other disorders might benefit people with a newly identified type of Charcot-Marie-Tooth disease (CMT) that may be a common recessive form of hereditary neuropathy. They are inviting people diagnosed with CMT but with no clear disease-causing mutation to help by joining a registry whose data are supporting further work. Genetic testing for this subtype will be offered to those who register. “This remarkable discovery has been possible because of…

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