Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation
Abstract
The Arg406Trp (R406W) missense mutation in the microtubule‐associated protein‐tau gene (MAPT) is a known cause of early‐onset dementia. Various dementia phenotypes have been described, including frontotemporal dementia (FTD), FTD with parkinsonism, and early‐onset Alzheimer disease (EOAD)‐like presentations.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Jun 03, 2013
- Source ID
- 10.1016/j.jalz.2013.02.011
Entities
People
- Adam C. Naj
- Brian W. Kunkle
- John R. Gilbert
- Margaret A. Pericak‐vance
- Martin A. Kohli
- Regina M. Carney
- Stephan Zuchner
Organizations
- Alzheimer's Association
- BrightFocus Foundation
- United States Department of Defense
- University of Miami