Cmt2e - a form of charcot-marie-tooth disease which is inherited in an autosomal dominant manner. It is caused by mutation(s) in the nefl gene, encoding neurofilament light polypeptide. It results in peripheral axonal neuropathy.
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Source: Data courtesy of the U.S. National Library of Medicine. Since the data might have changed, please query MeSH on Cmt2e for any updates.