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Paper Details

SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation.
Hum Mutat
73
2005
16p, CMT, CMT1C, Charcot-Marie-Tooth (CMT) disease, Charcot-Marie-Tooth disease, E3 ubiquitin ligase, E3 ubiquitin ligases, Hrs, LITAF, LITAF transcript, NEDD4, PPXY, RING finger motif-containing, SIMPLE, SIMPLE gene, TSG10, TSG101, WW, clathrin, control chromosomes, demyelinating, inherited peripheral neuropathies, neuropathies, patients, sporadic CMT1, ubiquitin, weakness and atrophy of distal limb muscles

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