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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Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: Doppler, Kathrin, Brockmann, Kathrin, Sedghi, Annahita, Wurster, Isabel, Volkmann, Jens, Oertel, Wolfgang H., Sommer, Claudia
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Neurology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6304446/
https://ncbi.nlm.nih.gov/pubmed/30619053
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2018.01094
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