Novel PSEN1 (P284S) Mutation Causes Alzheimer's Disease with Cerebellar Amyloid β-Protein Deposition

Background/Objective: AD-associated PSEN1 mutations exhibit high clinical heterogeneity. The discovery of these mutations and the analysis of their associations with cases such as EOAD should be critical to understanding AD's pathogenesis. Methods: We performed clinical analysis, neuroimaging,...

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Detalles Bibliográficos
Autores principales: Xia, Mingrong, Gao, Chenhao, Wang, Huayuan, Shang, Junkui, Liu, Ruijie, You, Yang, Zang, Weizhou, Zhang, Jiewen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933047/
https://www.ncbi.nlm.nih.gov/pubmed/35850649
http://dx.doi.org/10.2174/1567205019666220718151357

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933047/
https://www.ncbi.nlm.nih.gov/pubmed/35850649
http://dx.doi.org/10.2174/1567205019666220718151357

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