Article

Impaired Mitochondrial Mobility in Charcot-Marie-Tooth Disease

2020-11-06

Abstract excerpt

Charcot-Marie-Tooth (CMT) disease is the most commonly inherited neurological disorder, defined by progressive deterioration of the peripheral nerves. Clinical manifestations of CMT mutations are typically limited to peripheral neurons, the longest cells in the body. Currently, mutations in at least 80 different genes are associated with CMT and new mutations are regularly being discovered. A large portion of the...

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Literature Corpus work: cbf6dd30-ea64-5136-b4ab-65a1ad6be47a
DOI: 10.20944/preprints202011.0227.v1

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