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Altered CSF levels of monoamines in hereditary spastic paraparesis 10: A case series
OBJECTIVE: To perform a comprehensive clinical characterization and biochemical CSF profile analyses in 2 Swedish families with hereditary spastic paraparesis (HSP) 10 (SPG10) caused by 2 different mutations in the neuronal kinesin heavy chain gene (KIF5A). METHODS: Structured clinical assessment, g...
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| Publicado no: | Neurol Genet |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6659133/ https://ncbi.nlm.nih.gov/pubmed/31403080 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000344 |
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