Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A.

Published

Journal Article (Review)

Charcot-Marie-Tooth disease (CMT) is the most common form of hereditary peripheral neuropathy. The main axonal form of CMT, CMT2A, preferentially affects peripheral neurons with the longest neurites. CMT2A has been recently linked to mutations in the mitofusin 2 (Mfn2) gene. Mfn2 participates in mitochondrial fusion a process that together with mitochondrial fission, contributes to mitochondrial morphology. Many hypotheses have been postulated to understand how mutations in Mfn2 lead to CMT2A. In this review, we will describe the physiological role of Mfn2, the pathophysiology of CMT2A and current hypotheses about the deleterious role of mutant Mfn2 in neuronal function.

Full Text

Duke Authors

Cited Authors

  • Cartoni, R; Martinou, J-C

Published Date

  • August 2009

Published In

Volume / Issue

  • 218 / 2

Start / End Page

  • 268 - 273

PubMed ID

  • 19427854

Pubmed Central ID

  • 19427854

Electronic International Standard Serial Number (EISSN)

  • 1090-2430

Digital Object Identifier (DOI)

  • 10.1016/j.expneurol.2009.05.003

Language

  • eng

Conference Location

  • United States