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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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| Yayımlandı: | Amyotroph Lateral Scler Frontotemporal Degener |
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| Asıl Yazarlar: | , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2014
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| Konular: | |
| Online Erişim: | 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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