Longitudinal imaging in C9orf72 mutation carriers: Relationship to phenotype

Expansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), or mixtures of the two clinical phenotypes. Different imaging findings have been described for C9orf72-associated diseases in comparison with sporadic patients with the same phenotyp...

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Detalles Bibliográficos
Autores principales: Floeter, Mary Kay, Bageac, Devin, Danielian, Laura E., Braun, Laura E., Traynor, Bryan J., Kwan, Justin Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153604/
https://www.ncbi.nlm.nih.gov/pubmed/27995069
http://dx.doi.org/10.1016/j.nicl.2016.10.014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153604/
https://www.ncbi.nlm.nih.gov/pubmed/27995069
http://dx.doi.org/10.1016/j.nicl.2016.10.014

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