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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:Front Neurol
Glavni autori: Doppler, Kathrin, Brockmann, Kathrin, Sedghi, Annahita, Wurster, Isabel, Volkmann, Jens, Oertel, Wolfgang H., Sommer, Claudia
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2018
Teme:
Neurology
Online pristup: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
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items