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A C9ORF72 BAC mouse model recapitulates key epigenetic perturbations of ALS/FTD
BACKGROUND: Amyotrophic Lateral Sclerosis (ALS) is a fatal and progressive neurodegenerative disorder with identified genetic causes representing a significant minority of all cases. A GGGGCC hexanucleotide repeat expansion (HRE) mutation within the C9ORF72 gene has recently been identified as the m...
Autores principales: | Esanov, Rustam, Cabrera, Gabriela Toro, Andrade, Nadja S., Gendron, Tania F., Brown, Robert H., Benatar, Michael, Wahlestedt, Claes, Mueller, Christian, Zeier, Zane |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468954/ https://www.ncbi.nlm.nih.gov/pubmed/28606110 http://dx.doi.org/10.1186/s13024-017-0185-9 |
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