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...

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Detalles Bibliográficos
Autores principales: Bennion Callister, Janis, Pickering-Brown, Stuart M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2014
Materias:
Review
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

Internet

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

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