Cortical Frontoparietal Network Dysfunction in CHMP2B -Frontotemporal Dementia
Cortical Frontoparietal Network Dysfunction in CHMP2B -Frontotemporal Dementia
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Publisher
Switzerland: Frontiers Research Foundation
Journal title
Language
English
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Publisher
Switzerland: Frontiers Research Foundation
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Contents
A rare cause of inherited frontotemporal dementia (FTD) is a mutation in the
gene on chromosome 3 leading to the autosomal dominantly inherited FTD (
-FTD). Since
-FTD is clinically well-characterized, and patients show a distinct pattern of executive dysfunction, the condition offers possible insight in the early electroencephalographic (...
Alternative Titles
Full title
Cortical Frontoparietal Network Dysfunction in CHMP2B -Frontotemporal Dementia
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TN_cdi_doaj_primary_oai_doaj_org_article_cc78cd044125440b9c28ce0618e30014
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_cc78cd044125440b9c28ce0618e30014
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ISSN
1663-4365
E-ISSN
1663-4365
DOI
10.3389/fnagi.2021.714220
