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

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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Bibliographic Details
Main Authors: Yaling Jiang, Bin Jiao, Xinxin Liao, Xuewen Xiao, Xixi Liu, Lu Shen
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-09-01
Series:Frontiers in Aging Neuroscience
Subjects:
Alzheimer’s disease
hereditary amyloidosis
gelsolin
genetics
China
Online Access:https://www.frontiersin.org/article/10.3389/fnagi.2020.581524/full

Internet

https://www.frontiersin.org/article/10.3389/fnagi.2020.581524/full

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