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Normal Dopaminergic Nigrostriatal Innervation in SPG3A Hereditary Spastic Paraplegia
SPG3A/atlastin-1 gene mutations cause an autosomal dominant form of hereditary spastic paraplegia (SPG3A-HSP). We used positron emission tomography with [(11)C]DTBZ to assess nigrostriatal dopaminergic integrity in two unrelated adults with SPG3A-HSP due to the common SPG3A/atlastin-1 mutation, R239...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2008
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2743137/ https://ncbi.nlm.nih.gov/pubmed/19085270 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/01677060802337307 |
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