Mouse Models of C9orf72 Hexanucleotide Repeat Expansion in Amyotrophic Lateral Sclerosis/ Frontotemporal Dementia

The presence of hexanucleotide repeat expansion (HRE) in the first intron of the human C9orf72 gene is the most common genetic cause underlying both familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Studies aimed at elucidating the pathogenic mechanisms associated of C9...

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Detalles Bibliográficos
Autores principales: Batra, Ranjan, Lee, Chris W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498553/
https://www.ncbi.nlm.nih.gov/pubmed/28729824
http://dx.doi.org/10.3389/fncel.2017.00196

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498553/
https://www.ncbi.nlm.nih.gov/pubmed/28729824
http://dx.doi.org/10.3389/fncel.2017.00196

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