A novel p.Leu(381)Phe mutation in presenilin 1 is associated with very early onset and unusually fast progressing dementia as well as lysosomal inclusions typically seen in Kufs disease (Q39360964)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel p.Leu(381)Phe mutation in presenilin 1 is associated with very early onset and unusually fast progressing dementia as well as lysosomal inclusions typically seen in Kufs disease |
scientific article |
Statements
1 reference
A novel p.Leu(381)Phe mutation in presenilin 1 is associated with very early onset and unusually fast progressing dementia as well as lysosomal inclusions typically seen in Kufs disease (English)
1 reference
Stephan Zuchner
1 reference
Natalia Dolzhanskaya
1 reference
Michael A Gonzalez
1 reference
Fiorella Sperziani
1 reference
Shannon Stefl
1 reference
Jeffrey Messing
1 reference
Guang Y Wen
1 reference
Emil Alexov
1 reference
Milen Velinov
1 reference
1 January 2014
1 reference
1 reference
1 reference
Identifiers
1 reference