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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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Autors principals: Hall, DA, Jennings, D, Seibyl, J, Tassone, F, Marek, K
Format: Artigo
Idioma:Inglês
Publicat: 2010
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Accés en línia: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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