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Converging mechanisms in ALS and FTD: Disrupted RNA and protein homeostasis
Breakthrough discoveries identifying common genetic causes for amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) have transformed our view of these disorders. They share unexpectedly similar signatures, including dysregulation in common molecular players including TDP-43, FUS/TLS...
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| Publicat a: | Neuron |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4411085/ https://ncbi.nlm.nih.gov/pubmed/23931993 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2013.07.033 |
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