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Modeling the C9ORF72 repeat expansion mutation using human induced pluripotent stem cells
C9ORF72 repeat expansion is the most frequent causal genetic mutation giving rise to amyotrophic lateral sclerosis (ALS) and fronto‐temporal dementia (FTD). The relatively recent discovery of the C9ORF72 repeat expansion in 2011 and the complexity of the mutation have meant that animal models that s...
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| Publicado no: | Brain Pathol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8029270/ https://ncbi.nlm.nih.gov/pubmed/28585384 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bpa.12520 |
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