Cortical Frontoparietal Network Dysfunction in CHMP2B-Frontotemporal Dementia

A rare cause of inherited frontotemporal dementia (FTD) is a mutation in the CHMP2B gene on chromosome 3 leading to the autosomal dominantly inherited FTD (CHMP2B-FTD). Since CHMP2B-FTD is clinically well-characterized, and patients show a distinct pattern of executive dysfunction, the condition off...

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Detalles Bibliográficos
Autores principales: Musaeus, Christian Sandøe, Pedersen, Jette Stokholm, Kjær, Troels Wesenberg, Johannsen, Peter, Waldemar, Gunhild, Haverberg, Maria Joy Normann, Bacher, Theis, Nielsen, Jørgen Erik, Roos, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8475188/
https://www.ncbi.nlm.nih.gov/pubmed/34588974
http://dx.doi.org/10.3389/fnagi.2021.714220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8475188/
https://www.ncbi.nlm.nih.gov/pubmed/34588974
http://dx.doi.org/10.3389/fnagi.2021.714220

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