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Updated: Jan 31, 2026

Analyzing Mitochondrial Transport and Morphology in Human Induced Pluripotent Stem Cell-Derived Neurons in Hereditary Spastic Paraplegia
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Overlapping molecular pathological themes link Charcot-Marie-Tooth neuropathies and hereditary spastic paraplegias

Vincent Timmerman1, Virginia E Clowes, Evan Reid

  • 1Peripheral Neuropathy Group, Department of Molecular Genetics, VIB, Antwerpen, Belgium. vincent.timmerman@molgen.vib-ua.be

Experimental Neurology
|January 31, 2012
PubMed

Keywords:
ADARAxon degenerationCMAPCMTCNSCharcot–Marie–ToothERHMNHMSNHNPPHSANHSPHereditary neuropathyHereditary spastic paraplegiaNCVPIPNSSNAPautosomal dominantautosomal recessivecentral nervous systemcompound muscle action potentialsendoplasmic reticulumhereditary motor and sensory neuropathyhereditary motor neuropathyhereditary neuropathy with liability to pressure palsieshereditary sensory and autonomic neuropathyhereditary spastic paraplegianerve conduction velocityperipheral nervous systemphosphoinositidessensory nerve action potentials

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