Glial Cell Dysfunction in C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

Since the discovery of the chromosome 9 open reading frame 72 (C9orf72) repeat expansion mutation in 2011 as the most common genetic abnormality in amyotrophic lateral sclerosis (ALS, also known as Lou Gehrig’s disease) and frontotemporal dementia (FTD), progress in understanding the signaling pathw...

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Detalles Bibliográficos
Autores principales: Ghasemi, Mehdi, Keyhanian, Kiandokht, Douthwright, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912327/
https://www.ncbi.nlm.nih.gov/pubmed/33525344
http://dx.doi.org/10.3390/cells10020249

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912327/
https://www.ncbi.nlm.nih.gov/pubmed/33525344
http://dx.doi.org/10.3390/cells10020249

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