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FMR1 Gene Expansion and Scans without Evidence of Dopaminergic Deficits in Parkinsonism Patients
PURPOSE: To determine if patients with parkinsonism and fragile X mental retardation 1 (FMR1) gene expansions have a striatal dopamine deficit similar to Parkinson disease (PD) patients. SCOPE: The authors studied three patients with parkinsonism carrying small expansions in the FMR1 gene (41–60 CGG...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2963704/ https://ncbi.nlm.nih.gov/pubmed/20702130 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2010.07.006 |
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