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Explaining intermediate filament accumulation in giant axonal neuropathy
Giant axonal neuropathy (GAN)(1) is a rare autosomal recessive neurological disorder caused by mutations in the GAN gene that encodes gigaxonin, a member of the BTB/Kelch family of E3 ligase adaptor proteins.(1) This disease is characterized by the aggregation of Intermediate Filaments (IF)—cytoskel...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Landes Bioscience
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3927486/ https://ncbi.nlm.nih.gov/pubmed/25003002 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/rdis.25378 |
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