Analysis of common and rare VPS13C variants in late-onset Parkinson disease

OBJECTIVE: We aimed to study the role of coding VPS13C variants in a large cohort of patients with late-onset Parkinson disease (PD) (LOPD). METHODS: VPS13C and its untranslated regions were sequenced using targeted next-generation sequencing in 1,567 patients with PD and 1,667 controls from 3 cohor...

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Bibliografske podrobnosti
izdano v:Neurol Genet
Main Authors: Rudakou, Uladzislau, Ruskey, Jennifer A., Krohn, Lynne, Laurent, Sandra B., Spiegelman, Dan, Greenbaum, Lior, Yahalom, Gilad, Desautels, Alex, Montplaisir, Jacques Y., Fahn, Stanley, Waters, Cheryl H., Levy, Oren, Kehoe, Caitlin M., Narayan, Sushma, Dauvilliers, Yves, Dupré, Nicolas, Hassin-Baer, Sharon, Alcalay, Roy N., Rouleau, Guy A., Fon, Edward A., Gan-Or, Ziv
Format: Artigo
Jezik:Inglês
Izdano: Wolters Kluwer 2020
Teme:
Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6984134/
https://ncbi.nlm.nih.gov/pubmed/32042909
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000385
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