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Nuclear localization of SMN and FUS is not altered in fibroblasts from patients with sporadic ALS
BACKGROUND: Sporadic amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with no established biological marker. Recent observation of a reduced number of gems (survival motor neuron protein (SMN)-positive nuclear bodies) in cells from patients with familial ALS and the mouse mod...
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| Publicat a: | Amyotroph Lateral Scler Frontotemporal Degener |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4372808/ https://ncbi.nlm.nih.gov/pubmed/24809826 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/21678421.2014.907319 |
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