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DT‐02‐01: Loss‐of‐function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort
Author(s) -
Gijselinck Ilse,
Mossevelde Sara,
Sieben Anne,
Heeman Bavo,
Engelborghs Sebastiaan,
Vandenbulcke Mathieu,
Cuijt Ivy,
Broeck Marleen,
Peeters Karin,
Mattheijssens Maria,
Vandenberghe Rik,
Jonghe Peter,
Cras Patrick,
Deyn Peter P.,
Martin Jean-Jacques,
Cruts Marc,
Broeckhoven Christine
Publication year - 2015
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2015.08.157
Subject(s) - frontotemporal dementia , mutation , genetics , c9orf72 , frontotemporal lobar degeneration , cohort , loss function , exome sequencing , biology , medicine , gene , trinucleotide repeat expansion , allele , phenotype , dementia , disease
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