Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

OBJECTIVE: To assess the genetic contribution of TBK1, a gene implicated in amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), and FTD-ALS, in Belgian FTD and ALS patient cohorts containing a significant part of genetically unresolved patients. METHODS: We sequenced TBK1 in a hospit...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691687/
https://www.ncbi.nlm.nih.gov/pubmed/26581300
http://dx.doi.org/10.1212/WNL.0000000000002220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691687/
https://www.ncbi.nlm.nih.gov/pubmed/26581300
http://dx.doi.org/10.1212/WNL.0000000000002220

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