Alterations of Striatal Subregions in a Prion Protein Gene V180I Mutation Carrier Presented as Frontotemporal Dementia With Parkinsonism

OBJECTIVE: To explore the roles of striatal subdivisions in the pathogenesis of frontotemporal dementia with parkinsonism (FTDP) in a patient resulting from prion protein gene (PRNP) mutation. METHODS: This patient received clinical interviews and underwent neuropsychological assessments, genetic te...

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Detalles Bibliográficos
Autores principales: Chen, Zhongyun, Ma, Jinghong, Liu, Li, Liu, Shuying, Zhang, Jing, Chu, Min, Wang, Zhen, Chan, Piu, Wu, Liyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053668/
https://www.ncbi.nlm.nih.gov/pubmed/35493933
http://dx.doi.org/10.3389/fnagi.2022.830602

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053668/
https://www.ncbi.nlm.nih.gov/pubmed/35493933
http://dx.doi.org/10.3389/fnagi.2022.830602

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