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A novel KIF5A gene variant causes spastic paraplegia and cerebellar ataxia
Mutations in the kinesin family member 5A (KIF5A) gene are mainly associated with autosomal dominant spastic paraplegia 10 (SPG10). The additional complicated symptoms of SPG10 commonly include a wide spectrum. However, cerebellar ataxia is only noticed in a very few patients. Herein, we described a...
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| Publicado no: | Ann Clin Transl Neurol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6243379/ https://ncbi.nlm.nih.gov/pubmed/30480035 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.650 |
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