Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review.

Volume: 10, Issue: 1, Pages: 2
Published: Jan 9, 2018
Abstract
The MAPT c.1216C > T (p.Arg406Trp; R406W) mutation is a known cause of frontotemporal dementia with Parkinsonism linked to chromosome 17 tau with Alzheimer’s disease-like clinical features. We compiled clinical data from a new Swedish kindred with R406W mutation. Seven family members were followed longitudinally for up to 22 years. Radiological examinations were performed in six family members and neuropathological examinations in three. We...
Paper Details
Title
Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review.
Published Date
Jan 9, 2018
Volume
10
Issue
1
Pages
2
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