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SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis
The mutation of the spatacsin gene is the single most common cause of autosomal recessive hereditary spastic paraplegia with thin corpus callosum. Common clinical, pathological and genetic features between amyotrophic lateral sclerosis and hereditary spastic paraplegia motivated us to investigate 25...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2822627/ https://ncbi.nlm.nih.gov/pubmed/20110243 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awp325 |
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