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Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure
Hereditary spastic paraplegias are a clinically and genetically heterogeneous group of gait disorders. Their pathological hallmark is a length-dependent distal axonopathy of nerve fibers in the corticospinal tract. Involvement of other neurons can cause additional neurological symptoms, which define...
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| Main Authors: | , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
National Academy of Sciences
2013
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3612678/ https://ncbi.nlm.nih.gov/pubmed/23479643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1217197110 |
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