Dermal Phospho-Alpha-Synuclein Deposition in Patients With Parkinson's Disease and Mutation of the Glucocerebrosidase Gene

Heterozygous mutations in the glucocerebrosidase gene (GBA1) represent the most common genetic risk factor for Parkinson's disease (PD) and are histopathologically associated with a widespread load of alpha-synuclein in the brain. Therefore, PD patients with GBA1 mutations are a cohort of high...

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Detalles Bibliográficos
Autores principales: Doppler, Kathrin, Brockmann, Kathrin, Sedghi, Annahita, Wurster, Isabel, Volkmann, Jens, Oertel, Wolfgang H., Sommer, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304446/
https://www.ncbi.nlm.nih.gov/pubmed/30619053
http://dx.doi.org/10.3389/fneur.2018.01094

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304446/
https://www.ncbi.nlm.nih.gov/pubmed/30619053
http://dx.doi.org/10.3389/fneur.2018.01094

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