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A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A family
Lois Dankwa1, Jessica Richardson1, William W Motley1,2
1Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Journal of the Peripheral Nervous System : JPNS
|January 18, 2018
Abstract:
Dominant mutations in MFN2 cause a range of phenotypes, including severe, early-onset axonal neuropathy, "classical CMT2," and late-onset axonal neuropathies. We report a large family with an axonal polyneuropathy, with clinical onset in the 20s, followed by slow progression.
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