Loss ofTBK1is a frequent cause of frontotemporal dementia in a Belgian cohort-Reference-Cited by-同舟云学术

Loss ofTBK1is a frequent cause of frontotemporal dementia in a Belgian cohort

Published:2015-11-18 Issue:24 Volume:85 Page:2116-2125
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Gijselinck Ilse,Van Mossevelde Sara,van der Zee Julie,Sieben Anne,Philtjens Stéphanie,Heeman Bavo,Engelborghs Sebastiaan,Vandenbulcke Mathieu,De Baets Greet,Bäumer Veerle,Cuijt Ivy,Van den Broeck Marleen,Peeters Karin,Mattheijssens Maria,Rousseau Frederic,Vandenberghe Rik,De Jonghe Peter,Cras Patrick,De Deyn Peter P.,Martin Jean-Jacques,Cruts Marc,Van Broeckhoven Christine

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference39 articles.

1. The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

2. Molecular analysis and biochemical classification of TDP-43 proteinopathy

3. Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

4. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

5. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

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