Disruption of ER‐mitochondria tethering and signalling in C9orf72‐associated amyotrophic lateral sclerosis and frontotemporal dementia

Hexanucleotide repeat expansions in C9orf72 are the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). The mechanisms by which the expansions cause disease are not properly understood but a favoured route involves its translation into dipeptide repea...

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Detalles Bibliográficos
Autores principales: Gomez‐Suaga, Patricia, Mórotz, Gábor M., Markovinovic, Andrea, Martín‐Guerrero, Sandra M., Preza, Elisavet, Arias, Natalia, Mayl, Keith, Aabdien, Afra, Gesheva, Vesela, Nishimura, Agnes, Annibali, Ambra, Lee, Younbok, Mitchell, Jacqueline C., Wray, Selina, Shaw, Christopher, Noble, Wendy, Miller, Christopher C. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844122/
https://www.ncbi.nlm.nih.gov/pubmed/35026048
http://dx.doi.org/10.1111/acel.13549

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