Table 1.
Neurodegenerative disease | Mutant gene/disease protein |
---|---|
Hereditary spastic paraplegia | Kinesin heavy chain (Kif 5a) |
Familial motor neuron disease | Dynactin p150 subunit |
Charcot-Marie-Tooth disease type 2A | Kinesin Kif 1B β subunit |
Huntington’s disease | Huntingtin |
Familial amyotrophic lateral sclerosis | Superoxide dismutase 1 |
Parkinson’s disease and related synucleinopathies | α-synuclein |
Alzheimer’s disease | APP, presenilins, tau |
Neurodegenerative tauopathies | tau |
This table summarizes neurodegenerative diseases potentially linked to impairments in axonal transport as well as their mutant or disease proteins (see Roy et al15 for further details and additional citations).