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Glucose Hypometabolism Prompts RAN Translation and Exacerbates C9orf72-related ALS/FTD Phenotypes
The most prevalent genetic cause of both amyotrophic lateral sclerosis and frontotemporal dementia is a (GGGGCC)(n) nucleotide repeat expansion (NRE) occurring in the first intron of the C9orf72 gene (C9). Brain glucose hypometabolism is consistently observed in C9-NRE carriers, even at pre-symptoma...
Autores principales: | Nelson, A.T., Cicardi, M.E., Markandaiah, S.S., Han, J., Philp, N., Welebob, E., Haeusler, A.R., Pasinelli, P., Manfredi, G., Kawamata, H., Trotti, D. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274806/ https://www.ncbi.nlm.nih.gov/pubmed/37333144 http://dx.doi.org/10.1101/2023.06.07.544100 |
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