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Emerging Perspectives on Dipeptide Repeat Proteins in C9ORF72 ALS/FTD
The most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) is a hexanucleotide expansion in the chromosome 9 open reading frame 72 gene (C9ORF72). This hexanucleotide expansion consists of GGGGCC (G(4)C(2)) repeats that have been implicated to lead to thre...
Autores principales: | Schmitz, Alexander, Pinheiro Marques, João, Oertig, Irina, Maharjan, Niran, Saxena, Smita |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930069/ https://www.ncbi.nlm.nih.gov/pubmed/33679328 http://dx.doi.org/10.3389/fncel.2021.637548 |
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