Analyses Mutations in GSN, CST3, TTR, and ITM2B Genes in Chinese Patients With Alzheimer’s Disease

Amyloid protein deposition is a common mechanism of hereditary amyloidosis (HA) and Alzheimer’s disease (AD). Mutations of gelsolin (GSN), cystatin C (CST3), transthyretin (TTR), and integral membrane protein 2B (ITM2B) genes can lead to HA. But the relationship is unclear between these genes and AD...

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Detalles Bibliográficos
Autores principales: Jiang, Yaling, Jiao, Bin, Liao, Xinxin, Xiao, Xuewen, Liu, Xixi, Shen, Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533594/
https://www.ncbi.nlm.nih.gov/pubmed/33192475
http://dx.doi.org/10.3389/fnagi.2020.581524

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533594/
https://www.ncbi.nlm.nih.gov/pubmed/33192475
http://dx.doi.org/10.3389/fnagi.2020.581524

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