Frontotemporal dementia linked to chromosome 3 (FTD-3) - current concepts and the detection of a previously unknown branch of the Danish FTD-3 family

Author:

Lindquist S. G.,Braendgaard H.,Svenstrup K.,Isaacs A. M.,Nielsen J. E.,

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference21 articles.

1. Inheritance of frontotemporal dementia;Chow;Archives of Neurology,1999

2. The overlap of amyotrophic lateral sclerosis and frontotemporal dementia;Lomen-Hoerth;Neurology,2002

3. Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22;Wilhelmsen;American Journal of Human Genetics,1994

4. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein;Watts;Nature Genetics,2004

5. Mutations in progranulin cause tau-negative frontotemporal dementia;Baker;Nature,2006

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