ALS-FUS pathology revisited: singleton FUS mutations and an unusual case with both a FUS and TARDBP mutation

INTRODUCTION: Mutations in the FUS gene have been shown to be a rare cause of amyotrophic lateral sclerosis (ALS-FUS) and whilst well documented clinically and genetically there have been relatively few neuropathological studies.Recent work suggested a possible correlation between pathological featu...

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Detalles Bibliográficos
Autores principales: King, Andrew, Troakes, Claire, Smith, Bradley, Nolan, Matthew, Curran, Olimpia, Vance, Caroline, Shaw, Christopher E., Al-Sarraj, Safa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600255/
https://www.ncbi.nlm.nih.gov/pubmed/26452761
http://dx.doi.org/10.1186/s40478-015-0235-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600255/
https://www.ncbi.nlm.nih.gov/pubmed/26452761
http://dx.doi.org/10.1186/s40478-015-0235-x

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