Hypothesis and Theory: Roles of Arginine Methylation in C9orf72-Mediated ALS and FTD

Hexanucleotide repeat expansion (G4C2(n)) mutations in the gene C9ORF72 account for approximately 30% of familial cases of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), as well as approximately 7% of sporadic cases of ALS. G4C2(n) mutations are known to result in the product...

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Detalles Bibliográficos
Autores principales: Gill, Anna L., Premasiri, Alan S., Vieira, Fernando G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cellular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021787/
https://www.ncbi.nlm.nih.gov/pubmed/33833668
http://dx.doi.org/10.3389/fncel.2021.633668

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021787/
https://www.ncbi.nlm.nih.gov/pubmed/33833668
http://dx.doi.org/10.3389/fncel.2021.633668

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