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
|
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