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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Front Cell Neurosci
Autors principals: Schmitz, Alexander, Pinheiro Marques, João, Oertig, Irina, Maharjan, Niran, Saxena, Smita
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2021
Matèries:
Neuroscience
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7930069/
https://ncbi.nlm.nih.gov/pubmed/33679328
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2021.637548
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars