Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis

OBJECTIVE: Mutations in Fused in Sarcoma (FUS or TLS) are the fourth most prevalent in Western European familial amyotrophic lateral sclerosis (ALS) populations and have been associated with causing both early and very late disease onset. FUS aggregation, DNA repair deficiency, and genomic instabili...

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Detalles Bibliográficos
Autores principales: Naumann, Marcel, Peikert, Kevin, Günther, Rene, van der Kooi, Anneke J., Aronica, Eleonora, Hübers, Annemarie, Danel, Veronique, Corcia, Philippe, Pan‐Montojo, Francisco, Cirak, Sebahattin, Haliloglu, Göknur, Ludolph, Albert C., Goswami, Anand, Andersen, Peter M., Prudlo, Johannes, Wegner, Florian, Van Damme, Philip, Weishaupt, Jochen H., Hermann, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917314/
https://www.ncbi.nlm.nih.gov/pubmed/31682085
http://dx.doi.org/10.1002/acn3.50930

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917314/
https://www.ncbi.nlm.nih.gov/pubmed/31682085
http://dx.doi.org/10.1002/acn3.50930

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