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Motor dysfunction and neurodegeneration in a C9orf72 mouse line expressing poly-PR

A GGGGCC hexanucleotide repeat expansion in intron 1 of chromosome 9 open reading frame 72 (C9ORF72) gene is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia. Repeat-associated non-ATG translation of dipeptide repeat proteins (DPRs) contributes to the...

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Detalles Bibliográficos
Autores principales:	Hao, Zongbing, Liu, Liu, Tao, Zhouteng, Wang, Rui, Ren, Haigang, Sun, Hongyang, Lin, Zixuan, Zhang, Zhixiong, Mu, Chenchen, Zhou, Jiawei, Wang, Guanghui
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2019
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6606620/ https://www.ncbi.nlm.nih.gov/pubmed/31266945 http://dx.doi.org/10.1038/s41467-019-10956-w

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