Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review.
| Author | |
|---|---|
| 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. |
| Year of Publication |
:
2018
|
| Journal |
:
Alzheimer's research & therapy
|
| Volume |
:
10
|
| Issue |
:
1
|
| Number of Pages |
:
2
|
| Date Published |
:
2018
|
| DOI |
:
10.1186/s13195-017-0330-2
|
| Short Title |
:
Alzheimers Res Ther
|
| Download citation |
