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C9orf72 repeat expansions are a rare genetic cause of parkinsonism
The recently identified C9ORF72 gene accounts for a large proportion of amyotrophic lateral sclerosis and frontotemporal lobar degenerations. Since several forms of these disorders are associated with parkinsonism, we hypothesized that some patients with Parkinson’s disease or other forms of parkins...
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| Main Authors: | , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3984141/ https://ncbi.nlm.nih.gov/pubmed/23413259 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/aws357 |
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