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Journal article

Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia

Abstract:

Availability of data and materials: The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.Copyright © The Author(s) 2022. Background: Approximately a third of frontotemporal dementia (FTD) is genetic with mutations in three genes accounting for most of the inheritance: C9orf72, GRN, and MAPT. Impaired synaptic health is a common mechanism in all three genetic variants, so developing fluid biomarkers of this process could...

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Publication status:
Published
Peer review status:
Peer reviewed

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Role:
Author
ORCID:
0000-0002-7869-8192
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Role:
Author
ORCID:
0000-0002-2856-6060
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Role:
Author
ORCID:
0000-0002-9097-0152
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Role:
Author
ORCID:
0000-0002-1934-6162
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Role:
Author
ORCID:
0000-0003-1814-5024


Publisher:
BioMed Central
Journal:
Alzheimer's Research & Therapy More from this journal
Volume:
14
Issue:
1
Pages:
118-118
Article number:
118
Publication date:
2022-08-31
DOI:
EISSN:
1758-9193
ISSN:
1758-9193


Language:
English
Keywords:
Pubs id:
1279739
Local pid:
pubs:1279739
Source identifiers:
W4293771139
Deposit date:
2026-04-28
ARK identifier:
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