about
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion.
P50
description
onderzoeker
@nl
name
Veerle Bäumer
@ast
Veerle Bäumer
@en
Veerle Bäumer
@es
Veerle Bäumer
@sl
type
label
Veerle Bäumer
@ast
Veerle Bäumer
@en
Veerle Bäumer
@es
Veerle Bäumer
@sl
prefLabel
Veerle Bäumer
@ast
Veerle Bäumer
@en
Veerle Bäumer
@es
Veerle Bäumer
@sl
P106
P21
P31
P569
2000-01-01T00:00:00Z