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Hereditary spastic paraplegia SPG4: what is known and not known about the disease
Mutations in more than 70 distinct loci and more than 50 mutated gene products have been identified in patients with hereditary spastic paraplegias, a diverse group of neurological disorders characterized predominantly, but not exclusively, by progressive lower limb spasticity and weakness resulting...
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| Gepubliceerd in: | Brain |
|---|---|
| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4643622/ https://ncbi.nlm.nih.gov/pubmed/26094131 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awv178 |
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