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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Front Neurol
मुख्य लेखकों: Doppler, Kathrin, Brockmann, Kathrin, Sedghi, Annahita, Wurster, Isabel, Volkmann, Jens, Oertel, Wolfgang H., Sommer, Claudia
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Frontiers Media S.A. 2018
विषय:
Neurology
ऑनलाइन पहुंच: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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