Clinical and imaging findings in Parkinson disease associated with the A53E SNCA mutation

OBJECTIVE: To describe the clinical features and brain imaging findings of autosomal dominant Parkinson disease (PD) associated with a recently reported mutation in SNCA. METHODS: A Finnish family with PD in 3 successive generations, in accordance with an autosomal dominant inheritance pattern, was...

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Detalles Bibliográficos
Autores principales: Martikainen, Mika H., Päivärinta, Markku, Hietala, Marja, Kaasinen, Valtteri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811387/
https://www.ncbi.nlm.nih.gov/pubmed/27066564
http://dx.doi.org/10.1212/NXG.0000000000000027

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