Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
We identified in a cohort of patients with frontotemporal dementia (n = 481) or amyotrophic lateral sclerosis (n = 147), 10 index patients carrying a TBK1 loss of function mutation reducing TBK1 expression by 50%. Here, we describe the clinical and pathological characteristics of the 10 index patients and six of their affected relatives carrying a TBK1 mutation. Six TBK1 carriers were diagnosed with frontotemporal dementia, seven with amyotrophic lateral sclerosis, one with both clinical phenotypes and two with dementia unspecified. The mean age at onset of all 16 TBK1 carriers was 62.1 ± 8.9... Mehr ...
Verfasser: | |
---|---|
Dokumenttyp: | Artikel |
Erscheinungsdatum: | 2016 |
Verlag/Hrsg.: |
Oxford University Press
|
Schlagwörter: | Adult / Intercellular Signaling Peptides and Proteins / Male / Middle Aged / Mutation / Pedigree / Protein-Serine-Threonine Kinases / Proteins / Aged / Amyotrophic Lateral Sclerosis / Belgium / Cohort Studies / Female / Frontotemporal Dementia / Heterozygote / Humans |
Sprache: | Englisch |
Permalink: | https://search.fid-benelux.de/Record/base-26979866 |
Datenquelle: | BASE; Originalkatalog |
Powered By: | BASE |
Link(s) : | http://hdl.handle.net/2078.1/184277 |