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ALS mutations of FUS suppress protein translation and disrupt the regulation of nonsense-mediated decay
Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative disease characterized by preferential motor neuron death. Approximately 15% of ALS cases are familial, and mutations in the fused in sarcoma (FUS) gene contribute to a subset of familial ALS cases. FUS is a multifunctional protein...
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| Pubblicato in: | Proc Natl Acad Sci U S A |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
National Academy of Sciences
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6304956/ https://ncbi.nlm.nih.gov/pubmed/30455313 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1810413115 |
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