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Pathogenesis/genetics of frontotemporal dementia and how it relates to ALS
One of the most interesting findings in the field of neurodegeneration in recent years is tfche discovery of a genetic mutation in the C9orf72 gene, the most common mutation found to be causative of sporadic and familial frontotemporal lobar degeneration (FTLD), amyotrophic lateral sclerosis (ALS) a...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Academic Press
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221591/ https://www.ncbi.nlm.nih.gov/pubmed/24915640 http://dx.doi.org/10.1016/j.expneurol.2014.06.001 |