Neuronal Transcriptome from C9orf72 Repeat Expanded Human Tissue is Associated with Loss of C9orf72 Function

A hexanucleotide G(4)C(2) repeat expansion in C9orf72 is the most common genetic cause of familial and sporadic cases of amyotrophic lateral sclerosis (ALS) and frontotemporal degeneration (FTD). The mutation is associated with a reduction of C9orf72 protein and accumulation of toxic RNA and dipepti...

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Detalles Bibliográficos
Autores principales: Liu, Elaine Y., Russ, Jenny, Lee, Edward B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470232/
https://www.ncbi.nlm.nih.gov/pubmed/32905541

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470232/
https://www.ncbi.nlm.nih.gov/pubmed/32905541

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